ATRICURE CRYO1 CRYO-ABLATION PROBE
K-Number: K082074 · 2009-03-02
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Device Summary
Frequently Asked Questions
What is the ATRICURE CRYO1 CRYO-ABLATION PROBE?
ATRICURE CRYO1 CRYO-ABLATION PROBE is a medical device that received FDA 510(k) clearance on 2009-03-02. The listed applicant is AtriCure, Inc.. The 510(k) number is K082074.
When did ATRICURE CRYO1 CRYO-ABLATION PROBE receive FDA 510(k) clearance?
ATRICURE CRYO1 CRYO-ABLATION PROBE received FDA 510(k) clearance on 2009-03-02, under 510(k) number K082074.
Who is the listed applicant for ATRICURE CRYO1 CRYO-ABLATION PROBE?
The FDA 510(k) record lists AtriCure, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATRICURE CRYO1 CRYO-ABLATION PROBE?
The FDA product code for ATRICURE CRYO1 CRYO-ABLATION PROBE 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 AtriCure, 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: 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
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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