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

AVL 9180 ELECTROLYTE ANALYZER

K Number: K961458 · Decision Jun 12, 1996
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
28
Applicant Total
33
Review Days
58

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Basic Information

Device Name
AVL 9180 ELECTROLYTE ANALYZER
K Number
K961458
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1145
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avl Scientific Corp.
Date Received
April 15, 1996
Decision Date
June 12, 1996
Product Code
JFP
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
JFP Electrode, Ion Specific, Calcium

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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
K972733 AVL OMNI ANALYZER
K972673 AVL 9181 ELECTROLYTE ANALYZER
K963964 AVL COMPACT 3 PH/BLOOD GAS ANALYZER
Search all 33 clearances from Avl Scientific Corp. →