VISI-WIPE— 510(k) K884924

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K884924 for VISI-WIPE, Substantially Equivalent on 1989-01-31. Applicant: Visitec Co.. Device class: 1.

Clearance details

Applicant: Visitec Co.
Product code: Code HOF
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1988-11-28
Decision date: 1989-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

Download summary PDF View on FDA.gov ↗

More clearances from Visitec Co.

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K945738 — VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPE1995-02-14
K945172 — VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS1995-01-17
K942234 — VISITEC PRECISE-POINT1994-07-12

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