CANDELA CRYO-PROBE HOLDER— 510(k) K954872

Substantially Equivalent

Candela Laser Corp.

FDA 510(k) clearance K954872 for CANDELA CRYO-PROBE HOLDER, Substantially Equivalent on 1996-02-05. Applicant: Candela Laser Corp..

Clearance details

Applicant: Candela Laser Corp.
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 1995-10-24
Decision date: 1996-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayland, MA, US

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Adverse events under product code GEH

product code GEH

Death: 25
Injury: 351
Malfunction: 901
Total: 1,277

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.