CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4— 510(k) K910624

Name: FDA 510(k) clearance K910624
Creator: U.S. Food and Drug Administration
Published: 1992-01-17

Substantially Equivalent

Wr Medical Electronics Co.

FDA 510(k) clearance K910624 for CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4, Substantially Equivalent on 1992-01-17. Applicant: Wr Medical Electronics Co.. Device class: 1.

Clearance details

Applicant: Wr Medical Electronics Co.
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 1991-02-12
Decision date: 1992-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stillwater, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLN

view all

K072882 — PAIN VISION, MODEL PS-21002009-01-08
K030829 — VPT METER2003-12-05
K010981 — GSA GENITO SENSORY ANALYZER2001-09-20
K964622 — MEDI-DX 70001997-12-01
K964815 — AP-4000, AIR PULSE SENSORY STIMULATOR1997-09-04

More clearances from Wr Medical Electronics Co.

view all

K092809 — HRV ACQUIRE2010-10-19
K063560 — HILGER DUAL-STIM NERVE STIMULATOR2007-01-05
K000574 — IONTOPHORETIC DRUG DELIVERY ELECTRODE, IONTOPHORETIC ELECTRODE (ACTIVE)2000-08-09
K992874 — Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM1999-11-18
K895838 — BRACKMANN EMG MONITORING SYSTEM1990-03-27

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