LENZAR REMOTE ACQUISITION SYSTEM— 510(k) K941224

Name: FDA 510(k) clearance K941224
Creator: U.S. Food and Drug Administration
Published: 1994-12-09

Substantially Equivalent

Lenzar Electrooptics, Inc.

FDA 510(k) clearance K941224 for LENZAR REMOTE ACQUISITION SYSTEM, Substantially Equivalent on 1994-12-09. Applicant: Lenzar Electrooptics, Inc.. Device class: 1.

Clearance details

Applicant: Lenzar Electrooptics, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1994-03-14
Decision date: 1994-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riviera Beach, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMD

view all

K994329 — IIVS INTEGRATED IMAGE VIEWING STATION2000-05-26
K992698 — STENTOR, PAGEVIEW1999-10-25
K992426 — RAYPAX WEB CLINICAL SYSTEM1999-10-13
K992352 — ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.01999-09-29
K991537 — SAMSUNG RAYPAX SYSTEM1999-07-06

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