Medical Device Manufacturer · US , Charlton , MA

Karl Storz Endovision, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Karl Storz Endovision, Inc. has 1 FDA 510(k) cleared medical devices. Based in Charlton, US.

Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Karl Storz Endovision, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Karl Storz Endoscopy America, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Karl Storz Endovision, Inc.
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