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

FIBROGEN(FIBRIN SPLIT PRODUCT) ANTIGEN

K Number: K812298 · Decision Dec 17, 1981
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
27
Applicant Total
34
Review Days
125

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
FIBROGEN(FIBRIN SPLIT PRODUCT) ANTIGEN
K Number
K812298
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7320
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Syn-Kit, Inc.
Date Received
August 14, 1981
Decision Date
December 17, 1981
Product Code
GHH
Advisory Committee
Hematology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
GHH Fibrin Split Products

Similar 510(k) Clearances

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

View all

Other Clearances by Syn-Kit, Inc.

K Number Device Name
K861098 SEROIDEN STREPTO KIT 'EIKEN'
K861631 SLIDE CULTURE U 'EIKEN'
K854819 CPR SLIDE EIKEN
K854820 RA 80 EIKEN
K853276 ASO SLIDE EIKEN
K843758 UROPAPER EIKEN GK
K843753 UROPAPER EIKEN GP
K843754 UROPAPER EIKEN 7
K843760 UROPAPER EIKEN G
K843756 UROPAPER EIKEN 5
Search all 34 clearances from Syn-Kit, Inc. →