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FDA 510(k)

SERIES 2000 BEDSIDE PATIENT MONITOR

K-Number: K872354 · 1987-07-21

ApplicantMarquette Electronics, Inc.
Decision Date1987-07-21
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERIES 2000 BEDSIDE PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872354. 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 SERIES 2000 BEDSIDE PATIENT MONITOR?

SERIES 2000 BEDSIDE PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K872354.

When did SERIES 2000 BEDSIDE PATIENT MONITOR receive FDA 510(k) clearance?

SERIES 2000 BEDSIDE PATIENT MONITOR received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872354.

Who is the listed applicant for SERIES 2000 BEDSIDE PATIENT MONITOR?

The FDA 510(k) record lists Marquette Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIES 2000 BEDSIDE PATIENT MONITOR?

The FDA product code for SERIES 2000 BEDSIDE PATIENT MONITOR is 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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