Guidance for the Content of Premarket Notifications for Biopsy Devices Used in Gastroenterology and Urology From Food and Drug Administration (FDA) 🇺🇸 A guidance document providing premarket instructions for biopsy devices used in gastroenterology and urology. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on March 17, 2020 Other (Public Domain) 0 reuses 0 favorites
Checklist for Mechanical Lithotripters and Stone Dislodgers used in Gastroenterology and Urology From Food and Drug Administration (FDA) 🇺🇸 A guidance document for premarket mechanical lithotripters and stone dislodgers used in gastroenterology and urology. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on March 17, 2020 Other (Public Domain) 0 reuses 0 favorites
Gastroenterology and Urology Devices; Effective Date of Requirement for Premarket Approval of the Implanted Mechanical/Hydraulic Urinary Continence Device From Food and Drug Administration (FDA) 🇺🇸 Document number 00-24632. The Food and Drug Administration (FDA) is issuing a final rule to require the filing of a premarket approval application (PMA) or a notice of completion of a product development protocol (PDP) for the implanted mechanical/hydraulic urinary continence device, a generic… Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on September 26, 2000 Other (Public Domain) 0 reuses 0 favorites
Gastroenterology and Urology Devices; Reclassification of the Extracorporeal Shock Wave Lithotripter From Food and Drug Administration (FDA) 🇺🇸 Document number 00-20089. The Food and Drug Administration (FDA) is issuing a final rule to reclassify from class III to class II the extracorporeal shock wave lithotripter, when intended for use to fragment kidney and ureteral calculi. FDA is taking this action on its own initiative in order to… Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on August 9, 2000 Other (Public Domain) 0 reuses 0 favorites