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

BOEHRINGER MANNHEIM COAGUCHEK SYSTEM

K Number: K930454 · Decision Aug 5, 1993
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
179
Applicant Total
340
Review Days
190

Basic Information

Device Name
BOEHRINGER MANNHEIM COAGUCHEK SYSTEM
K Number
K930454
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
January 27, 1993
Decision Date
August 5, 1993
Product Code
JPA
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
JPA System, Multipurpose For In Vitro Coagulation Studies

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K983469 PRECISET SERUM PROTEINS CALIBRATOR
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