FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

S-357 VIDEO IMAGING SYSTEM

K Number: K972540 · Decision Sep 18, 1997
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
97
Applicant Total
25
Review Days
73

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Basic Information

Device Name
S-357 VIDEO IMAGING SYSTEM
K Number
K972540
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sopro
Date Received
July 7, 1997
Decision Date
September 18, 1997
Product Code
FET
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology

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Other Clearances by Sopro

K Number Device Name
K223470 C50
K121685 SOPROCARE
K103813 SOPRO 281
K092329 SOPIX 2
K092583 SOPROLIFE
K082796 SOPRO 184 CAMERA
K080122 SOPRO 670 ARTHROSCOPIC PUMP
K070783 SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR
K072912 SOPRO 225 DUAL HALOGEN LIGHT SOURCE
K070102 SOPRO 162 CAMERA
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