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

DIA THROMBIN DIA PLASTIN

K Number: K840802 · Decision May 1, 1984
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
17
Review Days
68

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Basic Information

Device Name
DIA THROMBIN DIA PLASTIN
K Number
K840802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Diatech, Inc.
Date Received
February 23, 1984
Decision Date
May 1, 1984
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

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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
K854090 DIATIMER-2 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
Search all 17 clearances from Diatech, Inc. →