FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

ADEPT INSTRUMENT POSITIONING ACCESSORY

K Number: K922626 · Decision Oct 19, 1992
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
16
Review Days
138

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Basic Information

Device Name
ADEPT INSTRUMENT POSITIONING ACCESSORY
K Number
K922626
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Andronic Devices, Ltd.
Date Received
June 3, 1992
Decision Date
October 19, 1992
Product Code
GAD
Advisory Committee
General, Plastic Surgery
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
GAD Retractor

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Other Clearances by Andronic Devices, Ltd.

K Number Device Name
K940812 INSIGHT ELECTRONIC ALIGNMENT INDICATOR
K934926 INSITE MODEL 20 & MODEL 15 INSUFFLATORS
K934928 INSITE FILTER & TUBING SET
K935381 KAPS POSITIONING ARM
K934124 AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM
K936308 ENDEX ENDOSCOPIC POSITIONING SYSTEM
K932253 ARTHROBOT BI-FOLD DRAPE
K922625 ADEPT ENDOSCOPIC POSITIONER
K911520 ARTHROBOT(TM) 75 (190 CM) GENERAL PURPOSE DRAPE
K911521 ARTHROBOT(TM) 96 (240 CM) DRAPE WITH 1 STRAP
Search all 16 clearances from Andronic Devices, Ltd. →