MEDDARS/ULTRA IMAGER RESPIRATION MODULE— 510(k) K812667

Name: FDA 510(k) clearance K812667
Creator: U.S. Food and Drug Administration
Published: 1981-10-23

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K812667 for MEDDARS/ULTRA IMAGER RESPIRATION MODULE, Substantially Equivalent on 1981-10-23. Applicant: Honeywell, Inc.. Device class: 2.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1981-09-21
Decision date: 1981-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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