ACCUTRAX, MODEL EPF840— 510(k) K982995

Name: FDA 510(k) clearance K982995
Creator: U.S. Food and Drug Administration
Published: 1998-12-04

Substantially Equivalent

Korr Medical Technologies, Inc.

FDA 510(k) clearance K982995 for ACCUTRAX, MODEL EPF840, Substantially Equivalent on 1998-12-04. Applicant: Korr Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Korr Medical Technologies, Inc.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1998-08-27
Decision date: 1998-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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