AQUEOUS PARACENTESIS PIPET— 510(k) K915808

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K915808 for AQUEOUS PARACENTESIS PIPET, Substantially Equivalent on 1992-03-19. Applicant: Visitec Co.. Device class: 1.

Clearance details

Applicant: Visitec Co.
Product code: Code KYG
Device class: Class 1
Regulation: 21 CFR 886.4360
Advisory panel: Ophthalmic
Date received: 1991-12-24
Decision date: 1992-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYG

K010353 — MED-LOGICS DISPOSABLE ALK TUBING2001-04-27
K003036 — TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,1010252000-12-22
K993591 — BLADEWORKS DISPOSABLE ALK TUBING1999-12-28
K981116 — SOVEREIGN CATARACT EXTRACTION SYSTEM1998-05-19
K980647 — EYE IRRIGATOR MODEL #20201998-05-15

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.