Medical Device Manufacturer · FR , Marseille

Sopro - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1997

Recent clearances: C50

Official Website
25
Total
25
Cleared
0
Denied

FDA 510(k) Regulatory Record - Sopro Gastroenterology & Urology ✕

3 devices
1-3 of 3
Cleared Mar 22, 2011
SOPRO 281
K103813 · NTN
Gastroenterology & Urology · 83d
Cleared Dec 03, 1997
S-357 VIDEO IMAGING SYSTEM
K973798 · FET
Gastroenterology & Urology · 58d
Cleared Sep 18, 1997
S-357 VIDEO IMAGING SYSTEM
K972540 · FET
Gastroenterology & Urology · 73d
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