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FDA 510(k)

COLORADO COLOR IMAGING RECORDER

K-Number: K902230 · 1990-06-19

ApplicantHoneywell, Inc.
Decision Date1990-06-19
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COLORADO COLOR IMAGING RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1990-06-19 under 510(k) number K902230. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLORADO COLOR IMAGING RECORDER?

COLORADO COLOR IMAGING RECORDER is a medical device that received FDA 510(k) clearance on 1990-06-19. The listed applicant is Honeywell, Inc.. The 510(k) number is K902230.

When did COLORADO COLOR IMAGING RECORDER receive FDA 510(k) clearance?

COLORADO COLOR IMAGING RECORDER received FDA 510(k) clearance on 1990-06-19, under 510(k) number K902230.

Who is the listed applicant for COLORADO COLOR IMAGING RECORDER?

The FDA 510(k) record lists Honeywell, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLORADO COLOR IMAGING RECORDER?

The FDA product code for COLORADO COLOR IMAGING RECORDER is DSF.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: DSF)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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