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FDA 510(k)

CRYOBALLOON ABLATION SYSTEM

K-Number: K101825 · 2010-09-29

Decision Date2010-09-29
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRYOBALLOON ABLATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is C2 Therapeutics. It received FDA 510(k) clearance on 2010-09-29 under 510(k) number K101825. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYOBALLOON ABLATION SYSTEM?

CRYOBALLOON ABLATION SYSTEM is a medical device that received FDA 510(k) clearance on 2010-09-29. The listed applicant is C2 Therapeutics. The 510(k) number is K101825.

When did CRYOBALLOON ABLATION SYSTEM receive FDA 510(k) clearance?

CRYOBALLOON ABLATION SYSTEM received FDA 510(k) clearance on 2010-09-29, under 510(k) number K101825.

Who is the listed applicant for CRYOBALLOON ABLATION SYSTEM?

The FDA 510(k) record lists C2 Therapeutics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRYOBALLOON ABLATION SYSTEM?

The FDA product code for CRYOBALLOON ABLATION SYSTEM is GEH.

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 C2 Therapeutics 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: GEH)

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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