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

MOPSO BUFFER

K Number: K792574 · Decision Jan 21, 1980
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
6
Applicant Total
27
Review Days
39

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Basic Information

Device Name
MOPSO BUFFER
K Number
K792574
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Electrophoresis Corp. of America
Date Received
December 13, 1979
Decision Date
January 21, 1980
Product Code
JCC
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
JCC Ph Buffer

Similar 510(k) Clearances

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

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Other Clearances by Electrophoresis Corp. of America

K Number Device Name
K802396 GENERAL PROCEDURE AGAROSE FILM
K792548 ALKALINE PHOSPHATASE MARKER
K792547 AGAROSE BARBITAL BUFFER
K792551 ALKALINE PHOSPHATASE REAGENT
K792553 AGAROSE BARBITAL-EDTA BUFFER
K792550 PONCEAU S STAIN SET
K792549 FAT RED 7B STAIN SET
K792552 AMIDO BLACK 10B STAIN
K791656 ENZYME STABILIZING REAGENT (ESR)
K791655 CPK ISOENZYME REAGENT
Search all 27 clearances from Electrophoresis Corp. of America →