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FDA 510(k)

PATIENT MONITOR #RM-100

K-Number: K831817 · 1983-10-31

ApplicantHoneywell, Inc.
Decision Date1983-10-31
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR #RM-100 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K831817. 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 PATIENT MONITOR #RM-100?

PATIENT MONITOR #RM-100 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Honeywell, Inc.. The 510(k) number is K831817.

When did PATIENT MONITOR #RM-100 receive FDA 510(k) clearance?

PATIENT MONITOR #RM-100 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K831817.

Who is the listed applicant for PATIENT MONITOR #RM-100?

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 #RM-100?

The FDA product code for PATIENT MONITOR #RM-100 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-AK855125PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEMK851888APM DISPOS. BLOOD PRESSURE TRANSDUCERK851496ECG MONITOR MODEL RM102

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Related Devices (Code: DRT)

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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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