ARVEE APNEA MONITOR, MODEL 2400— 510(k) K891676

Name: FDA 510(k) clearance K891676
Creator: U.S. Food and Drug Administration
Published: 1989-09-06

Substantially Equivalent

Arvee Medical, Inc.

FDA 510(k) clearance K891676 for ARVEE APNEA MONITOR, MODEL 2400, Substantially Equivalent on 1989-09-06. 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: 1989-03-21
Decision date: 1989-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Battle Creek, MI, US

Download summary PDF View on FDA.gov ↗

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