FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

P.R.G. GUIDEWIRE PLACEMENT SYSTEM

K Number: K903036 · Decision Nov 19, 1990
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
23
Review Days
131

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Basic Information

Device Name
P.R.G. GUIDEWIRE PLACEMENT SYSTEM
K Number
K903036
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Applicant
Applied Medical Technologies
Date Received
July 11, 1990
Decision Date
November 19, 1990
Product Code
KGC
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KGC Tube, Gastro-Enterostomy

Similar 510(k) Clearances

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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
K960232 ENDOSCOPIC ACCESS DEVICE
K945618 GASTROINTESTINAL TUBES & ACCESSORIES
K946140 PRG BUTTON
K923488 GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY
Search all 23 clearances from Applied Medical Technologies →