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FDA 510(k)

CENTRAL STATION MONITORING SYSTEM

K-Number: K761291 · 1976-12-28

ApplicantAbbott Laboratories
Decision Date1976-12-28
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL STATION MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1976-12-28 under 510(k) number K761291. 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 MONITORING SYSTEM?

CENTRAL STATION MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1976-12-28. The listed applicant is Abbott Laboratories. The 510(k) number is K761291.

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

CENTRAL STATION MONITORING SYSTEM received FDA 510(k) clearance on 1976-12-28, under 510(k) number K761291.

Who is the listed applicant for CENTRAL STATION MONITORING SYSTEM?

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

What is the FDA product code for CENTRAL STATION MONITORING SYSTEM?

The FDA product code for CENTRAL STATION MONITORING SYSTEM 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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