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

DIATIMER-2 BLOOD PLASMA CLOT TIMING INSTRUMENT

K Number: K854090 · Decision Jan 6, 1986
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
17
Review Days
91

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Basic Information

Device Name
DIATIMER-2 BLOOD PLASMA CLOT TIMING INSTRUMENT
K Number
K854090
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Diatech, Inc.
Date Received
October 7, 1985
Decision Date
January 6, 1986
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

Similar 510(k) Clearances

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

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Other Clearances by Diatech, Inc.

K Number Device Name
K881685 FIBRINOGENTEST-O
K854938 COASCREENER/DIASCREENERBLOOD PLASMA TIMING INST.
K854089 DIATIMER-1 BLOOD PLASMA CLOT TIMING INSTRUMENT
K842286 DIA T1, T2 & T3
K841523 OWREN'S VERONAL BUFFERR
K841462 HEPARIN COAGULATION CONTROL PLASMA 1-
K841366 DIA FIBRIN
K841365 DIA REPTIN
K841461 COAGULATION CONTROL PLASMA LEVEL 1/2/3
K840802 DIA THROMBIN DIA PLASTIN
Search all 17 clearances from Diatech, Inc. →