FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

SELECTOR

K Number: K925129 · Decision Apr 23, 1993
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
17
Review Days
192

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Basic Information

Device Name
SELECTOR
K Number
K925129
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Spembly Medical , Ltd.
Date Received
October 13, 1992
Decision Date
April 23, 1993
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

Similar 510(k) Clearances

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Other Clearances by Spembly Medical , Ltd.

K Number Device Name
K903303 SPEMBLY MEDICAL 242 CRYOUNIT/SERIES 242 CRYOPROBES
K901974 SELECTOR ULTRASONIC SURGICAL ASPIRATOR
K882568 130 CRYO UNIT & ASSOC. CRYOPROBES & SPRAY
K882962 SERIES 40 & SERIES 42 CRYOPROBES (R SERIES)
K882963 SPEMBLY MEDICAL 142 CRYO UNIT
K874367 VARIOUS CARDIAC CRYOPROBES HAVING DIA. & COS. DIFF
K840497 OBSTETRIC PULSAR TWO CHANNEL TENS
K832385 CRYOPROBES MC-1400-CRYOSURG-CONSOLE
K832334 CRYOMEDICS 5000 CRYOSURGICAL CONSOLE
K832140 CRYOMEDICS 5000 CRYOPROBES
Search all 17 clearances from Spembly Medical , Ltd. →