FDA 510(k) clearance · back to tracker

AtriCure cryoICE cryo-ablation probe (CRYO3), AtriCure cryoICE cryoFORM cryo-ablation probe (CRYOF)

AtriCure, Inc. cleared K180137 on 2018-02-15, decision: substantially equivalent

K-number

K180137

Sponsor

AtriCure, Inc.

Device

AtriCure cryoICE cryo-ablation probe (CRYO3), AtriCure cryoICE cryoFORM cryo-ablation probe (CRYOF)

Class

Class II

Decision

Substantially Equivalent

Decision date

2018-02-15

Product code

GEH

Advisory committee

General, Plastic Surgery

Medical specialty

General, Plastic Surgery

Regulation number

878.4350

Official FDA record

Open K180137on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.