BCLEAR— 510(k) K021762

Substantially Equivalent

Lumenis, Inc.

FDA 510(k) clearance K021762 for BCLEAR, Substantially Equivalent on 2002-08-23. Applicant: Lumenis, Inc.. Device class: 2.

Clearance details

Applicant: Lumenis, Inc.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 2002-05-29
Decision date: 2002-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

Download summary PDF View on FDA.gov ↗

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