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FDA 510(k)

CENTRAL STATION MONITOR

K-Number: K812271 · 1981-08-31

ApplicantDatascope Corp.
Decision Date1981-08-31
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL STATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812271. 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 CENTRAL STATION MONITOR?

CENTRAL STATION MONITOR is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Datascope Corp.. The 510(k) number is K812271.

When did CENTRAL STATION MONITOR receive FDA 510(k) clearance?

CENTRAL STATION MONITOR received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812271.

Who is the listed applicant for CENTRAL STATION MONITOR?

The FDA 510(k) record lists Datascope Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRAL STATION MONITOR?

The FDA product code for CENTRAL STATION 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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