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

CPK REAGENT SET, NAD REDUCTION

K Number: K781719 · Decision Nov 3, 1978
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
107
Review Days
23

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CPK REAGENT SET, NAD REDUCTION
K Number
K781719
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Medical Analysis Systems, Inc.
Date Received
October 11, 1978
Decision Date
November 3, 1978
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

Similar 510(k) Clearances

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

View all

Other Clearances by Medical Analysis Systems, Inc.

K Number Device Name
K042717 MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL
K041194 ABBOTT ARCHITECT STAT TROPONIN I LIQUID ASSAYED CARDIAC MARKER CONTROL LEVEL L, M AND H
K040880 MAS CARDIOIMMUNE TL LIQUID ASSAYED CARDIAC MARKER CONTROL, LEVELS 1,2 AND 3
K032826 MAS PAR TDM
K032335 MAS CARDIOIMMUNE PROBNP, MAS CARDIOIMMUNE TL
K031890 MAS BILIRUBIN LIQUID ASSAYED BILIRUBIN CONTROL
K031441 URICHEMTRAK LIQUID ASSAYED URINE CONTROL
K031392 MAS TOX AMMONIA CONTROLLIQUID ASSAYED TOX AMMONIA CONTROL
K031364 MAS CARDIOLMMUNE PROBNP LIQUID ASSAYED CARDIAC MARKER CONTROL LEVEL 1, 2 AND 3
K030942 MAS CHEMTRAK H & DADE MONI-TROL H LIQUID ASSAYED CHEMISTRY CONTROL
Search all 107 clearances from Medical Analysis Systems, Inc. →