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FDA 510(k)

AM 420 MICROPROCESSOR

K-Number: K810163 · 1981-03-05

ApplicantHoneywell, Inc.
Decision Date1981-03-05
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AM 420 MICROPROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-03-05 under 510(k) number K810163. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AM 420 MICROPROCESSOR?

AM 420 MICROPROCESSOR is a medical device that received FDA 510(k) clearance on 1981-03-05. The listed applicant is Honeywell, Inc.. The 510(k) number is K810163.

When did AM 420 MICROPROCESSOR receive FDA 510(k) clearance?

AM 420 MICROPROCESSOR received FDA 510(k) clearance on 1981-03-05, under 510(k) number K810163.

Who is the listed applicant for AM 420 MICROPROCESSOR?

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 AM 420 MICROPROCESSOR?

The FDA product code for AM 420 MICROPROCESSOR is DXG.

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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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