FDA 510(k) clearance · back to tracker

AblatePal Radiofrequency Ablation System

Compal Electronics, Inc. cleared K223135 on 2023-06-30, decision: substantially equivalent

K-number

K223135

Sponsor

Compal Electronics, Inc.

Device

AblatePal Radiofrequency Ablation System

Class

Class II

Decision

Substantially Equivalent

Decision date

2023-06-30

Product code

GEI

Advisory committee

General, Plastic Surgery

Medical specialty

General, Plastic Surgery

Regulation number

878.4400

Official FDA record

Open K223135on 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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Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

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