FIBEROPTIC ILLUMINATED INSTRUMENTS— 510(k) K934269

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K934269 for FIBEROPTIC ILLUMINATED INSTRUMENTS, Substantially Equivalent on 1994-05-17. Applicant: Visitec Co.. Device class: 2.

Clearance details

Applicant: Visitec Co.
Product code: Code HJM
Device class: Class 2
Regulation: 21 CFR 886.1945
Advisory panel: Ophthalmic
Date received: 1993-08-31
Decision date: 1994-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HJM

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K950529 — PEREGRINE DIFFUSION LIGHT PIPE1995-06-07
K945877 — WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT1995-03-02
K931072 — HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE1994-11-10
K933445 — DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)1994-09-23

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.