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FDA 510(k)

DUAL TRACE PATIENT MONITOR 116,118,120

K-Number: K810179 · 1981-02-25

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

Device Summary

DUAL TRACE PATIENT MONITOR 116,118,120 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 K810179. 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 DUAL TRACE PATIENT MONITOR 116,118,120?

DUAL TRACE PATIENT MONITOR 116,118,120 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 K810179.

When did DUAL TRACE PATIENT MONITOR 116,118,120 receive FDA 510(k) clearance?

DUAL TRACE PATIENT MONITOR 116,118,120 received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810179.

Who is the listed applicant for DUAL TRACE PATIENT MONITOR 116,118,120?

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 DUAL TRACE PATIENT MONITOR 116,118,120?

The FDA product code for DUAL TRACE PATIENT MONITOR 116,118,120 is 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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