FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD

K Number: K090109 · Decision Jun 24, 2009
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
7
Review Days
160

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Basic Information

Device Name
BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD
K Number
K090109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Epocal, Inc.
Date Received
January 15, 2009
Decision Date
June 24, 2009
Product Code
CGA
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
CGA Glucose Oxidase, Glucose

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Other Clearances by Epocal, Inc.

K Number Device Name
K200107 epoc Blood Analysis System
K171247 epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test
K113726 EPOC CHLORIDE TEST AND EPOC CREATININE TEST
K093297 EPOC BGEM, EPOC READER, EPOC HOST, EPOC CARE-FILL CAPILLARY TUBE
K092849 BLOOD COLLECTION TUBE SAMPLES FOR USE WITH POINT OF CARE BLOOD ANALYZER
K061597 EPOC BLOOD ANALYSIS SYSTEM