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

DIA FIBRIN

K Number: K841366 · Decision Jun 1, 1984
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
27
Applicant Total
17
Review Days
60

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Basic Information

Device Name
DIA FIBRIN
K Number
K841366
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7340
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Diatech, Inc.
Date Received
April 2, 1984
Decision Date
June 1, 1984
Product Code
KQJ
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
KQJ System, Fibrinogen Determination

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KQJ), 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
K854090 DIATIMER-2 BLOOD PLASMA CLOT TIMING INSTRUMENT
K842286 DIA T1, T2 & T3
K841523 OWREN'S VERONAL BUFFERR
K841462 HEPARIN COAGULATION CONTROL PLASMA 1-
K841365 DIA REPTIN
K841461 COAGULATION CONTROL PLASMA LEVEL 1/2/3
K840802 DIA THROMBIN DIA PLASTIN
Search all 17 clearances from Diatech, Inc. →