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

AVL OMNI ANALYZER

K Number: K954018 · Decision Oct 5, 1995
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
38
Applicant Total
33
Review Days
41

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Basic Information

Device Name
AVL OMNI ANALYZER
K Number
K954018
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5620
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avl Scientific Corp.
Date Received
August 25, 1995
Decision Date
October 5, 1995
Product Code
GKR
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
GKR System, Hemoglobin, Automated

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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. →