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FDA 510(k)

COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4

K-Number: K082051 · 2008-10-16

Decision Date2008-10-16
Product CodeGXD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4 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 2008-10-16 under 510(k) number K082051. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4?

COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4 is a medical device that received FDA 510(k) clearance on 2008-10-16. The listed applicant is Cosman Medical, Inc.. The 510(k) number is K082051.

When did COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4 receive FDA 510(k) clearance?

COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4 received FDA 510(k) clearance on 2008-10-16, under 510(k) number K082051.

Who is the listed applicant for COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4?

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 G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4?

The FDA product code for COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4 is GXD.

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: GXD)

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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