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

AVL OMNI ANALYZER

K Number: K972733 · Decision Sep 9, 1997
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
33
Review Days
50

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Basic Information

Device Name
AVL OMNI ANALYZER
K Number
K972733
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avl Scientific Corp.
Date Received
July 21, 1997
Decision Date
September 9, 1997
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 Avl Scientific Corp.

K Number Device Name
K001632 OPTI-CHECK PLUS MULTI-ANALYTE CONTROL, MODEL HC7009
K000103 AVL OPTI R ANALYZER
K993837 AVL OPTI CRITICAL CARE ANALYZER
K990092 AVL OMNI MODULAR ANALYZER
K984299 AVL OPTI CRITICAL CARE ANALYZER
K974784 AVL OPTI CRITICAL CARE ANALYZER
K974822 AVL OPTI-CHECK PH/ BLOOD GAS/ ELECTROLYTE/THB/ SO2 CONTROL
K972673 AVL 9181 ELECTROLYTE ANALYZER
K963964 AVL COMPACT 3 PH/BLOOD GAS ANALYZER
K961458 AVL 9180 ELECTROLYTE ANALYZER
Search all 33 clearances from Avl Scientific Corp. →