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

SOPRO 61D

K Number: K031593 · Decision Sep 16, 2003
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
25
Review Days
118

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Basic Information

Device Name
SOPRO 61D
K Number
K031593
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
May 21, 2003
Decision Date
September 16, 2003
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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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
Search all 25 clearances from Sopro →