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

SIGMA DIAGNOSTICS CO2ALKALINE BUFFER

K Number: K963538 · Decision Oct 11, 1996
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
27
Applicant Total
164
Review Days
37

Basic Information

Device Name
SIGMA DIAGNOSTICS CO2ALKALINE BUFFER
K Number
K963538
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIGMA DIAGNOSTICS, INC.
Date Received
September 4, 1996
Decision Date
October 11, 1996
Product Code
JFL
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JFL Ph Rate Measurement, Carbon-Dioxide

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K013544 SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 2, MODEL A8096
K013545 SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 3, MODEL A8221
K012410 INFINITY HBA KIT, MODELS 537-A, 537-B
K010652 SIGMA DIAGNOSTICS SIGMA-CAL, MODEL S2936
K010158 THROMBOMAX-HS WITH CALCIUM, MODEL T6540
K003267 SIGMA DIAGNOSTICS AUTO D-DIMER, MODEL CRS126-A
K003329 SIGMA DIANOSTICS AUTO D-DIMER CONTROL LEVEL 2, MODEL A5217
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