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FDA 510(k)

PATIENT MONITOR CM111, 112

K-Number: K810178 · 1981-02-25

ApplicantHoneywell, Inc.
Decision Date1981-02-25
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR CM111, 112 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K810178. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITOR CM111, 112?

PATIENT MONITOR CM111, 112 is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Honeywell, Inc.. The 510(k) number is K810178.

When did PATIENT MONITOR CM111, 112 receive FDA 510(k) clearance?

PATIENT MONITOR CM111, 112 received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810178.

Who is the listed applicant for PATIENT MONITOR CM111, 112?

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 PATIENT MONITOR CM111, 112?

The FDA product code for PATIENT MONITOR CM111, 112 is DSK.

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Related Devices (Code: DSK)

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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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