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

SOPRO 670 ARTHROSCOPIC PUMP

K Number: K080122 · Decision Jul 11, 2008
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
25
Review Days
176

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Basic Information

Device Name
SOPRO 670 ARTHROSCOPIC PUMP
K Number
K080122
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sopro
Date Received
January 17, 2008
Decision Date
July 11, 2008
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

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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
K070783 SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR
K072912 SOPRO 225 DUAL HALOGEN LIGHT SOURCE
K070102 SOPRO 162 CAMERA
K031593 SOPRO 61D
Search all 25 clearances from Sopro →