Medical Device Manufacturer · FR , Antony

Plancon Instruments - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1996

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Plancon Instruments Ophthalmic ✕

3 devices

1-3 of 3

Cleared Apr 15, 1998

PLANCON MICROLAMELLAR KERATOME EVOLUTION

Ophthalmic · 35d

Cleared Mar 31, 1997

PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES)

Ophthalmic · 56d

Cleared Apr 26, 1996

PLANCON MIRCOLAMELLAR KERATOME

Ophthalmic · 88d