Molectron Medical Nd:yag Laser, Model 8000

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K833480 ↗

FDA Product Code

LNK

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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See all devices from Cooper Lasersonics, Inc. →