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FDA 510(k)

CADHEALTH SYSTEM, MODEL CHP-001

K-Number: K002514 · 2001-05-31

Decision Date2001-05-31
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CADHEALTH SYSTEM, MODEL CHP-001 is the device name listed in this FDA 510(k) record. The listed applicant is Caduceus Health Care , Ltd.. It received FDA 510(k) clearance on 2001-05-31 under 510(k) number K002514. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADHEALTH SYSTEM, MODEL CHP-001?

CADHEALTH SYSTEM, MODEL CHP-001 is a medical device that received FDA 510(k) clearance on 2001-05-31. The listed applicant is Caduceus Health Care , Ltd.. The 510(k) number is K002514.

When did CADHEALTH SYSTEM, MODEL CHP-001 receive FDA 510(k) clearance?

CADHEALTH SYSTEM, MODEL CHP-001 received FDA 510(k) clearance on 2001-05-31, under 510(k) number K002514.

Who is the listed applicant for CADHEALTH SYSTEM, MODEL CHP-001?

The FDA 510(k) record lists Caduceus Health Care , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CADHEALTH SYSTEM, MODEL CHP-001?

The FDA product code for CADHEALTH SYSTEM, MODEL CHP-001 is DRG.

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.

Related Devices (Code: DRG)

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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