E*NET NEUROMONITORING SYSTEM— 510(k) K930080

Name: FDA 510(k) clearance K930080
Creator: U.S. Food and Drug Administration
Published: 1993-10-19

Substantially Equivalent

Physiometrix, Inc.

FDA 510(k) clearance K930080 for E*NET NEUROMONITORING SYSTEM, Substantially Equivalent on 1993-10-19. Applicant: Physiometrix, Inc.. Device class: 2.

Clearance details

Applicant: Physiometrix, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1993-01-07
Decision date: 1993-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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