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FDA 510(k)

APM DISPOS. BLOOD PRESSURE TRANSDUCER

K-Number: K851888 · 1985-08-06

ApplicantHoneywell, Inc.
Decision Date1985-08-06
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

APM DISPOS. BLOOD PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1985-08-06 under 510(k) number K851888. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APM DISPOS. BLOOD PRESSURE TRANSDUCER?

APM DISPOS. BLOOD PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1985-08-06. The listed applicant is Honeywell, Inc.. The 510(k) number is K851888.

When did APM DISPOS. BLOOD PRESSURE TRANSDUCER receive FDA 510(k) clearance?

APM DISPOS. BLOOD PRESSURE TRANSDUCER received FDA 510(k) clearance on 1985-08-06, under 510(k) number K851888.

Who is the listed applicant for APM DISPOS. BLOOD PRESSURE TRANSDUCER?

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 APM DISPOS. BLOOD PRESSURE TRANSDUCER?

The FDA product code for APM DISPOS. BLOOD PRESSURE TRANSDUCER is DRS.

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Related Devices (Code: DRS)

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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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