ARVEE APNEA MONITOR, MODEL 4800— 510(k) K900730

Name: FDA 510(k) clearance K900730
Creator: U.S. Food and Drug Administration
Published: 1990-06-14

Substantially Equivalent

Arvee Medical, Inc.

FDA 510(k) clearance K900730 for ARVEE APNEA MONITOR, MODEL 4800, Substantially Equivalent on 1990-06-14. Applicant: Arvee Medical, Inc.. Device class: 2.

Clearance details

Applicant: Arvee Medical, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1990-02-15
Decision date: 1990-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Battle Creek, MI, US

Download summary PDF View on FDA.gov ↗

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