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

MICROSAMPLE COAGULATION ANALYZER

K Number: K943153 · Decision Mar 24, 1995
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
48
Applicant Total
37
Review Days
267

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Basic Information

Device Name
MICROSAMPLE COAGULATION ANALYZER
K Number
K943153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5400
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio/Data Corp.
Date Received
June 30, 1994
Decision Date
March 24, 1995
Product Code
GKP
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
GKP Instrument, Coagulation, Automated

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Other Clearances by Bio/Data Corp.

K Number Device Name
K001891 MICROSAMPLE COAGULATION ANALYZER, MODEL MCA 310-C
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
K853078 CITREX III
Search all 37 clearances from Bio/Data Corp. →