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

PACIFIC HEMOSTASIS THROMBOPLASTIN D

K Number: K994100 · Decision Feb 18, 2000
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
29
Review Days
77

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Basic Information

Device Name
PACIFIC HEMOSTASIS THROMBOPLASTIN D
K Number
K994100
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pacific Hemostasis
Date Received
December 3, 1999
Decision Date
February 18, 2000
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.

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Other Clearances by Pacific Hemostasis

K Number Device Name
K000679 THROMBOSTRATE CONTROL PLASMAS
K992130 PACIFIC HEMOSTASIS THROMBOSCREEN 400C
K992279 HEPARIN CONTROL PLASMA LEVEL 2
K992278 HEPARIN CONTROL PLASMA LEVEL 1
K991321 PACIFIC HEMOSTASIS THROMBOSCREEN 200
K990046 PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR VIII DEFICIENT PLASMA
K984130 COAGULATION CONTROL LEVEL 2 (ABNORMAL)
K984129 COAGULATION CONTROL LEVEL 1 (NORMAL)
K984131 COAGULATION CONTROL LEVEL 3 (ABNORMAL)
K972627 PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR V DEFICIENT PLASMA (THROMBOSDREEN BRAND) (100056)
Search all 29 clearances from Pacific Hemostasis →