ANEFIN, MODEL 100— 510(k) K033028

Substantially Equivalent

Axon Medical

FDA 510(k) clearance K033028 for ANEFIN, MODEL 100, Substantially Equivalent on 2005-07-22. Applicant: Axon Medical. Device class: 2.

Clearance details

Applicant: Axon Medical
Product code: Code CBN
Device class: Class 2
Regulation: 21 CFR 868.5430
Advisory panel: Anesthesiology
Date received: 2003-09-26
Decision date: 2005-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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