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FDA 510(k)

CENTRYSYSTEM 3 WITH CHARTS/BP OPTION

K-Number: K925522 · 1994-09-30

Decision Date1994-09-30
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CENTRYSYSTEM 3 WITH CHARTS/BP OPTION is the device name listed in this FDA 510(k) record. The listed applicant is C.G.H. Medical, Inc.. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K925522. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRYSYSTEM 3 WITH CHARTS/BP OPTION?

CENTRYSYSTEM 3 WITH CHARTS/BP OPTION is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is C.G.H. Medical, Inc.. The 510(k) number is K925522.

When did CENTRYSYSTEM 3 WITH CHARTS/BP OPTION receive FDA 510(k) clearance?

CENTRYSYSTEM 3 WITH CHARTS/BP OPTION received FDA 510(k) clearance on 1994-09-30, under 510(k) number K925522.

Who is the listed applicant for CENTRYSYSTEM 3 WITH CHARTS/BP OPTION?

The FDA 510(k) record lists C.G.H. Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRYSYSTEM 3 WITH CHARTS/BP OPTION?

The FDA product code for CENTRYSYSTEM 3 WITH CHARTS/BP OPTION is KOC.

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 C.G.H. Medical, 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 11 devices →

Related Devices (Code: KOC)

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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