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

ENDOSCOPIC ACCESS DEVICE

K Number: K960232 · Decision Mar 21, 1996
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
23
Review Days
64

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Basic Information

Device Name
ENDOSCOPIC ACCESS DEVICE
K Number
K960232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Applied Medical Technologies
Date Received
January 17, 1996
Decision Date
March 21, 1996
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 Applied Medical Technologies

K Number Device Name
K971434 A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICE
K972478 PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES
K973893 AMT BALLOON STOMA MEASURING DEVICES, AMT BALLOON MEASURING DEVICE, AMT BALLOON MEASURING DEVICE WITH STOP VALVE, AMY BAE
K971757 LOW PROFILE FEEDING SET ACCESSORY
K971758 CAUTERIZATION SMOKE EVACUATOR
K961345 DOMED PERCUTANEOUS ENDOSCOPIC GASTROSTOMY(P.E.G.) FEEDING TUBE
K945618 GASTROINTESTINAL TUBES & ACCESSORIES
K946140 PRG BUTTON
K923488 GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY
K923692 STOMA MEASURING DEVICE
Search all 23 clearances from Applied Medical Technologies →