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Apparatus, Cutting, Radiofrequency, Electrosurgical, Ac-Powered

FDA product code PUL · 4 cleared devices

Class 2 Ophthalmic
Regulation
21 CFR 886.4100
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2017-06-02 – 2023-04-11

Used to perform anterior capsulotomy during cataract surgery

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