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

AGGRECETIN

K Number: K760893 · Decision Jan 12, 1977
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
37
Applicant Total
37
Review Days
77

Basic Information

Device Name
AGGRECETIN
K Number
K760893
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5700
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
BIO/DATA CORP.
Date Received
October 27, 1976
Decision Date
January 12, 1977
Product Code
JOZ
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
JOZ System, Automated Platelet Aggregation

Similar 510(k) Clearances

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

View all

Other Clearances by BIO/DATA CORP.

K Number Device Name
K001891 MICROSAMPLE COAGULATION ANALYZER, MODEL MCA 310-C
K943153 MICROSAMPLE COAGULATION ANALYZER
K893650 PLATELET AGGREGATION PROFILER MODEL PAP-4C
K881150 KINETIC FIBRINOGEN ASSAY
K873382 PLATELET EXTRACT REAGENT
K860751 VON WILLEBRAND FAC. DEFIC. ABNORMAL CONTROL PLASMA
K860342 MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP
K854546 MICROSAMPLE COAGULATION ANALYSER MODEL 110P
K853897 CITREX H
K853246 CALCIUM CHLORIDE
Search all 37 clearances from BIO/DATA CORP. →