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FDA 510(k)

COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA

K-Number: K060799 · 2006-05-02

Decision Date2006-05-02
Product CodeGXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Cosman Medical, Inc.. It received FDA 510(k) clearance on 2006-05-02 under 510(k) number K060799. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA?

COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA is a medical device that received FDA 510(k) clearance on 2006-05-02. The listed applicant is Cosman Medical, Inc.. The 510(k) number is K060799.

When did COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA receive FDA 510(k) clearance?

COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA received FDA 510(k) clearance on 2006-05-02, under 510(k) number K060799.

Who is the listed applicant for COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA?

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

What is the FDA product code for COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA?

The FDA product code for COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA is GXI.

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 Cosman 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.

Related Devices (Code: GXI)

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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