VISITEC SCLERAL PLUG— 510(k) K945114

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K945114 for VISITEC SCLERAL PLUG, Substantially Equivalent on 1995-02-23. Applicant: Visitec Co.. Device class: 2.

Clearance details

Applicant: Visitec Co.
Product code: Code LXP
Device class: Class 2
Regulation: 21 CFR 886.4155
Advisory panel: Ophthalmic
Date received: 1994-10-18
Decision date: 1995-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

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More clearances from Visitec Co.

K953394 — VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}1995-10-12
K945738 — VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPE1995-02-14
K945172 — VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS1995-01-17
K942234 — VISITEC PRECISE-POINT1994-07-12
K934269 — FIBEROPTIC ILLUMINATED INSTRUMENTS1994-05-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.