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FDA 510(k)

PHYSIOLOGIC RECORDER

K-Number: K810696 · 1981-03-27

ApplicantHoneywell, Inc.
Decision Date1981-03-27
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGIC 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 1981-03-27 under 510(k) number K810696. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIOLOGIC RECORDER?

PHYSIOLOGIC RECORDER is a medical device that received FDA 510(k) clearance on 1981-03-27. The listed applicant is Honeywell, Inc.. The 510(k) number is K810696.

When did PHYSIOLOGIC RECORDER receive FDA 510(k) clearance?

PHYSIOLOGIC RECORDER received FDA 510(k) clearance on 1981-03-27, under 510(k) number K810696.

Who is the listed applicant for PHYSIOLOGIC 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 PHYSIOLOGIC RECORDER?

The FDA product code for PHYSIOLOGIC RECORDER is DPS.

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Other records listing Honeywell, Inc. as applicant

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K902230COLORADO COLOR IMAGING RECORDERK863100CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECORK853501HONEYWELL ELECTRONIC VENTILATOR EV-AK855125PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEMK851888APM DISPOS. BLOOD PRESSURE TRANSDUCERK851496ECG MONITOR MODEL RM102

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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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