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FDA 510(k)

CENTRAL MONITORING SYSTEM

K-Number: K772152 · 1977-11-28

ApplicantBurdick Corp.
Decision Date1977-11-28
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1977-11-28 under 510(k) number K772152. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL MONITORING SYSTEM?

CENTRAL MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Burdick Corp.. The 510(k) number is K772152.

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

CENTRAL MONITORING SYSTEM received FDA 510(k) clearance on 1977-11-28, under 510(k) number K772152.

Who is the listed applicant for CENTRAL MONITORING SYSTEM?

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

What is the FDA product code for CENTRAL MONITORING SYSTEM?

The FDA product code for CENTRAL MONITORING SYSTEM is DXG.

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Other records listing Burdick Corp. 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.

K942565ALTAIR-DISC RECORDERK941351BURDICK PRO2 OXIMETERK903565E560 ELECTROCARDIOGRAPHK904032ELITE II ELECTROCARDIOGRAPHK900729NEOSERV 824K885085ERGOMED 840/ERGOMED 840L

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Related Devices (Code: DXG)

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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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