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FDA 510(k)

SERIES 7200 TRANSPORT/REMOTE ACQUISITION MONITOR

K-Number: K860734 · 1986-11-06

Decision Date1986-11-06
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERIES 7200 TRANSPORT/REMOTE ACQUISITION 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 1986-11-06 under 510(k) number K860734. 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 SERIES 7200 TRANSPORT/REMOTE ACQUISITION MONITOR?

SERIES 7200 TRANSPORT/REMOTE ACQUISITION MONITOR is a medical device that received FDA 510(k) clearance on 1986-11-06. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K860734.

When did SERIES 7200 TRANSPORT/REMOTE ACQUISITION MONITOR receive FDA 510(k) clearance?

SERIES 7200 TRANSPORT/REMOTE ACQUISITION MONITOR received FDA 510(k) clearance on 1986-11-06, under 510(k) number K860734.

Who is the listed applicant for SERIES 7200 TRANSPORT/REMOTE ACQUISITION 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 7200 TRANSPORT/REMOTE ACQUISITION MONITOR?

The FDA product code for SERIES 7200 TRANSPORT/REMOTE ACQUISITION MONITOR is DPS.

Related Clinical Trials

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.

Other records listing Marquette Electronics, 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.

View all 82 devices →

Related Devices (Code: DPS)

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.

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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