K252529

Moses 200 D/F/L Laser Fiber (M0068130100); Moses 365 D/F/L Laser Fiber (M0068130110); Moses 550 D/F/L Laser Fiber (M0068130120)

510(k) number: K252529
Device name: Moses 200 D/F/L Laser Fiber (M0068130100); Moses 365 D/F/L Laser Fiber (M0068130110); Moses 550 D/F/L Laser Fiber (M0068130120)
Applicant: Boston Scientific Corporation MA · US
Product code: GEX — Powered Laser Surgical Instrument
Decision date: 2025-10-30
Date received: 2025-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: General, Plastic Surgery

Also available from FDA: K252529.pdf

Official FDA record: K252529

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.