VISC X-VITREOUS ASPIRATING & CUT. INSTR— 510(k) K760684

Name: FDA 510(k) clearance K760684
Creator: U.S. Food and Drug Administration
Published: 1976-10-05

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K760684 for VISC X-VITREOUS ASPIRATING & CUT. INSTR, Substantially Equivalent on 1976-10-05. Applicant: Varian Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code HKP
Device class: Class 2
Regulation: 21 CFR 886.4150
Advisory panel: Ophthalmic
Date received: 1976-09-20
Decision date: 1976-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HKP

view all

K952558 — AARON VAC 21997-03-19
K950056 — THE GRIESHABER AXIAL CUTTER1995-05-05
K950287 — UNIVIT PROBE1995-04-10
K896622 — VISITEC VITRECTOMY UNIT1990-04-04
K890595 — MENTOR ANTERIOR SEGMENT VITRECTOR1989-04-17

More clearances from Varian Assoc., Inc.

view all

K000922 — PROTON VISION2000-05-24
K992762 — BRACHYVISION 6.02000-03-09
K992751 — SOMAVISION2000-02-16
K992753 — CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM1999-09-03
K990085 — MILLENNIUM MLC -1201999-02-08

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