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FDA 510(k)

PATIENT MONITOR MODEL RM-300

K-Number: K850794 · 1985-04-18

ApplicantHoneywell, Inc.
Decision Date1985-04-18
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR MODEL RM-300 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1985-04-18 under 510(k) number K850794. The device is classified under product code DTR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITOR MODEL RM-300?

PATIENT MONITOR MODEL RM-300 is a medical device that received FDA 510(k) clearance on 1985-04-18. The listed applicant is Honeywell, Inc.. The 510(k) number is K850794.

When did PATIENT MONITOR MODEL RM-300 receive FDA 510(k) clearance?

PATIENT MONITOR MODEL RM-300 received FDA 510(k) clearance on 1985-04-18, under 510(k) number K850794.

Who is the listed applicant for PATIENT MONITOR MODEL RM-300?

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 MODEL RM-300?

The FDA product code for PATIENT MONITOR MODEL RM-300 is DTR.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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