Medical Device Manufacturer · US , Walker , MI

Visitec Co. - FDA 510(k) Cleared Devices

49 submissions · 49 cleared · Since 1979

Total

Cleared

Denied

Visitec Co. has 49 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 49 cleared submissions from 1979 to 1995. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Visitec Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Visitec Co.

49 devices

1-12 of 49

Cleared Oct 12, 1995

VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}

VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPE

K945738 · HMT

General Hospital · 83d

Cleared Jan 17, 1995

VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS

K945172 · HQX

Ophthalmic · 88d

Cleared Jul 12, 1994

VISITEC PRECISE-POINT

K942234 · GAP

General & Plastic Surgery · 64d

Cleared May 17, 1994

FIBEROPTIC ILLUMINATED INSTRUMENTS

General & Plastic Surgery · 52d

Cleared Dec 27, 1993

VISI-SPEAR EYE SPONGE

K933872 · HOZ

Ophthalmic · 143d

Cleared Nov 04, 1992

OPHTHALMIC FLUID DISTRIBUTION SETS

K923972 · FPK

General Hospital · 89d

Cleared Oct 20, 1992

VISITEC MICROSURGICAL SUTURE

K922530 · GAR

General & Plastic Surgery · 145d

Cleared Sep 30, 1992

VISITEC ASPIRATING SYRINGE

K923645 · FMF

General Hospital · 71d

Cleared Mar 19, 1992

AQUEOUS PARACENTESIS PIPET

K915808 · KYG

Ophthalmic · 86d

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Visitec Co. - FDA 510(k) Cleared Devices

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