OMNIVAC (VACUUM ELECTRODE SYSTEM)— 510(k) K861039

Name: FDA 510(k) clearance K861039
Creator: U.S. Food and Drug Administration
Published: 1986-09-26

Substantially Equivalent

Physio Technology, Inc.

FDA 510(k) clearance K861039 for OMNIVAC (VACUUM ELECTRODE SYSTEM), Substantially Equivalent on 1986-09-26. Applicant: Physio Technology, Inc.. Device class: 2.

Clearance details

Applicant: Physio Technology, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1986-03-18
Decision date: 1986-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Topeka, KS, US

Download summary PDF View on FDA.gov ↗

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