VISITEC MAGNIFYING SPECTACLES— 510(k) K844038

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K844038 for VISITEC MAGNIFYING SPECTACLES, Substantially Equivalent on 1984-11-29. Applicant: Visitec Co.. Device class: 1.

Clearance details

Applicant: Visitec Co.
Product code: Code HOI
Device class: Class 1
Regulation: 21 CFR 886.5840
Advisory panel: Ophthalmic
Date received: 1984-10-16
Decision date: 1984-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOI

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K931328 — PYRAMID SUNGLASSES/PYRAMID READING GLASSES1993-08-10
K910329 — SUNGLASSES1991-03-12
K854854 — SYSTEMS OF SIGHT LOW VISION EYEWARE1986-02-04

More clearances from Visitec Co.

K953394 — VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}1995-10-12
K945114 — VISITEC SCLERAL PLUG1995-02-23
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.