FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

Y-GT TEST, Y-GLUTAMYL TRANSFERASE TEST

K Number: K800769 · Decision Apr 24, 1980
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
51
Applicant Total
82
Review Days
17

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Basic Information

Device Name
Y-GT TEST, Y-GLUTAMYL TRANSFERASE TEST
K Number
K800769
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1360
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Sclavo, Inc.
Date Received
April 7, 1980
Decision Date
April 24, 1980
Product Code
JQB
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
JQB Kinetic Method, Gamma-Glutamyl Transpeptidase

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K895822 TOTAL BILIRUBIN L.F.
K895847 CREATININE 340 (ENZYMATIC)
K880049 CHOLINESTERASE - BUTYRYTHIOCHOLINE SUBSTRATE
K880199 CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE
K873496 ATYPICAL CHOLINESTERASE
K884035 SAITRON 430 RANDOM ACCESS CHEMISTRY ANALYZER
Search all 82 clearances from Sclavo, Inc. →