FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

THROMBOPLASTIN

K Number: K884855 · Decision Jan 30, 1989
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
20
Review Days
73

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
THROMBOPLASTIN
K Number
K884855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Precision Biologicals, Inc.
Date Received
November 18, 1988
Decision Date
January 30, 1989
Product Code
GJS
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
GJS Test, Time, Prothrombin

Similar 510(k) Clearances

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

View all

Other Clearances by Precision Biologicals, Inc.

K Number Device Name
K981173 CRYO CHECK FACTOR XI DEFICIENT PLASMA, MODEL FDP11-10 (1.OML) AND FDP11-15 (1.5ML)
K982062 CRYO-CHECK PNP PLATELET LYSATE, MODEL PNP-10
K981174 CRYO CHECK FACTOR XII DEFICIENT PLASMA MODEL FDP12-10 (1.0ML) AND FDP12-15 (1.5ML)
K971219 CRYO CHECK INR VALIDATION SET
K971222 CRYO CHECK APC RESISTANT PLASMA
K971223 CRYO CHECK FACTOR V DEFICIENT PLASMA
K971227 CRYO CHECK FACTOR X DEFICIENT PLASMA
K971226 CRYO CHECK FACTOR IX DEFICIENT PLASMA
K971225 CRYO CHECK FACTOR VIII DEFICIENT PLASMA
K971224 CRYO CHECK FACTOR VII DEFICIENT PLASMA
Search all 20 clearances from Precision Biologicals, Inc. →