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

HEMOLYSE

K Number: K781121 · Decision Aug 14, 1978
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
28
Applicant Total
27
Review Days
42

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
HEMOLYSE
K Number
K781121
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.8540
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Electrophoresis Corp. of America
Date Received
July 3, 1978
Decision Date
August 14, 1978
Product Code
GGK
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GGK Products, Red-Cell Lysing Products

Similar 510(k) Clearances

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

View all

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 →