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

CENTOCOR AGGRESTAT, COLLAGEN REAGENT, CONTROL REAGENT

K Number: K954997 · Decision Jan 24, 1996
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
37
Applicant Total
3
Review Days
84

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Basic Information

Device Name
CENTOCOR AGGRESTAT, COLLAGEN REAGENT, CONTROL REAGENT
K Number
K954997
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5700
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Centocor, Inc.
Date Received
November 1, 1995
Decision Date
January 24, 1996
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.

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Other Clearances by Centocor, Inc.

K Number Device Name
K963803 CENTOCOR CA 15-3 RIA MODEL NO. 800-033
K820499 FITC ANTI-RABIES MONOCLONAL GLOBULIN