COLORADO COLOR IMAGING RECORDER— 510(k) K902230

Name: FDA 510(k) clearance K902230
Creator: U.S. Food and Drug Administration
Published: 1990-06-19

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K902230 for COLORADO COLOR IMAGING RECORDER, Substantially Equivalent on 1990-06-19. Applicant: Honeywell, Inc.. Device class: 1.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1990-05-17
Decision date: 1990-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, 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.