FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SOPRO 162 CAMERA

K Number: K070102 · Decision Feb 20, 2007
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
25
Review Days
41

Basic Information

Device Name
SOPRO 162 CAMERA
K Number
K070102
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
January 10, 2007
Decision Date
February 20, 2007
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
K031593 SOPRO 61D
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