LIGHT-PEN SYSTEM FOR QUANTI. ANALY.— 510(k) K772158

Name: FDA 510(k) clearance K772158
Creator: U.S. Food and Drug Administration
Published: 1977-11-22

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K772158 for LIGHT-PEN SYSTEM FOR QUANTI. ANALY., Substantially Equivalent on 1977-11-22. Applicant: Varian Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1977-11-16
Decision date: 1977-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DXG

view all

K253092 — Argos Infinity (Rev. 1.0)2026-02-13
K251275 — VitalStream ART Connect; VitalStream-Hemo2025-09-26
K232048 — Cogent Hemodynamic Monitoring System; Cogent HMS2023-12-20
K212529 — Hypotension Decision Assist Model HDA-OR22021-11-23
K192169 — PulsioFlex Monitoring System with ProAQT Sensor2020-04-30

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.