Karl Storz Endoscopy America Inc 2151 E Grand Ave El Segundo Ca 90245 Pma Numberp050027 Supplement Numbers030 Date Received02 16 2022 Decision Date03 17 2022 Product Code Oay Advisory Committee Gastroenterology Urology Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Karl Storz Endoscopy America Inc 2151 E Grand Ave El Segundo Ca 90245 Pma Numberp050027 Supplement Numbers030 Date Received02 16 2022 Decision Date03 17 2022 Product Code Oay Advisory Committee Gastroenterology Urology Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P050027S030 KARL STORZ ENDOSCOPY-AMERICA, INC.2151 E. Grand Ave.el Segundo, CA 90245 PMA NumberP050027 Supplement NumberS030 Date Received02/16/2022 Decision Date03/17/2022 Product Code OAY  Advisory Committee Gastroenterology/Urology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	KARL STORZ D-Light C PDD System	2022-03-17