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

LIPOPROTEIN STAIN

K Number: K781122 · Decision Aug 31, 1978
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
0
Applicant Total
27
Review Days
59

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Basic Information

Device Name
LIPOPROTEIN STAIN
K Number
K781122
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.1850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Electrophoresis Corp. of America
Date Received
July 3, 1978
Decision Date
August 31, 1978
Product Code
HZG
Advisory Committee
Hematology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
HZG Oil Red O

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
K792574 MOPSO BUFFER
K792550 PONCEAU S STAIN SET
K792549 FAT RED 7B STAIN SET
K792552 AMIDO BLACK 10B STAIN
K791656 ENZYME STABILIZING REAGENT (ESR)
Search all 27 clearances from Electrophoresis Corp. of America →