FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AVOXIMETER 4000

K Number: K951485 · Decision Nov 6, 1995
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
7
Applicant Total
3
Review Days
221

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Basic Information

Device Name
AVOXIMETER 4000
K Number
K951485
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3220
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
A-Vox Systems, Inc.
Date Received
March 30, 1995
Decision Date
November 6, 1995
Product Code
JKS
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
JKS Spectral Absorb. Curve, Oxyhemoglobin, Carboxyhemoglobin, Carbon-Monoxide

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JKS), ordered by most recent decision date.

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Other Clearances by A-Vox Systems, Inc.

K Number Device Name
K932954 AVOXIMETER
K922075 AVOXIMETER