BLSI VENTILATION MONITOR— 510(k) K810547

Name: FDA 510(k) clearance K810547
Creator: U.S. Food and Drug Administration
Published: 1981-03-11

Substantially Equivalent

Bunnell Life Systems, Inc.

FDA 510(k) clearance K810547 for BLSI VENTILATION MONITOR, Substantially Equivalent on 1981-03-11. Applicant: Bunnell Life Systems, Inc.. Device class: 2.

Clearance details

Applicant: Bunnell Life Systems, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1981-03-02
Decision date: 1981-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.