COSMAN CSK RF CANNULA; COSMAN RFK RF CANNULA
K-Number: K060799 · 2006-05-02
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Device Summary
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
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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