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

MODEL AM 722

K Number: K810203 · Decision Feb 10, 1981
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
28
Applicant Total
23
Review Days
18

Basic Information

Device Name
MODEL AM 722
K Number
K810203
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1145
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
APPLIED MEDICAL TECHNOLOGIES
Date Received
January 23, 1981
Decision Date
February 10, 1981
Product Code
JFP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JFP Electrode, Ion Specific, Calcium

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JFP), ordered by most recent decision date.

View all

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 →