K827408Substantially Equivalent

Ultra Imager

Name: K827408 Ultra Imager
Creator: Honeywell, Inc.
Published: 1982-10-04
License: https://open.fda.gov/license/

Honeywell, Inc., Minneapolis MN / Traditional, Substantially Equivalent

FDA source

K827408 is the FDA 510(k) clearance record for ULTRA IMAGER, cleared for Honeywell, Inc. on 1982-10-04. FDA records list 69 510(k) clearances for Honeywell, Inc., from 1976-10-13 to 1990-06-19. As of 2026-09-10, FDA records show no recalls naming K827408.

Clearance record

Decision date: 1982-10-04
Received: 1982-07-28 (68 days to decision)
Review panel: Unknown
Applicant: Honeywell, Inc. Honeywell Plz., Minneapolis MN
Third party review: No