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FDA 510(k)

PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM

K-Number: K855125 · 1986-03-26

ApplicantHoneywell, Inc.
Decision Date1986-03-26
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1986-03-26 under 510(k) number K855125. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM?

PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1986-03-26. The listed applicant is Honeywell, Inc.. The 510(k) number is K855125.

When did PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM receive FDA 510(k) clearance?

PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM received FDA 510(k) clearance on 1986-03-26, under 510(k) number K855125.

Who is the listed applicant for PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM?

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 PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM?

The FDA product code for PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM is DRT.

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Other records listing Honeywell, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K902230COLORADO COLOR IMAGING RECORDERK863100CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECORK853501HONEYWELL ELECTRONIC VENTILATOR EV-AK851888APM DISPOS. BLOOD PRESSURE TRANSDUCERK851496ECG MONITOR MODEL RM102K850794PATIENT MONITOR MODEL RM-300

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Related Devices (Code: DRT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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