MEDDARS/ULTRA IMAGER PULSE/PHON MODULE— 510(k) K811626

Name: FDA 510(k) clearance K811626
Creator: U.S. Food and Drug Administration
Published: 1981-07-01

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K811626 for MEDDARS/ULTRA IMAGER PULSE/PHON MODULE, Substantially Equivalent on 1981-07-01. Applicant: Honeywell, Inc.. Device class: 1.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code DQC
Device class: Class 1
Regulation: 21 CFR 870.2390
Advisory panel: Cardiovascular
Date received: 1981-06-09
Decision date: 1981-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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