PHYSIOMETRIX CABLE ADAPTER MODIFICATION— 510(k) K935260

Name: FDA 510(k) clearance K935260
Creator: U.S. Food and Drug Administration
Published: 1993-12-23

Substantially Equivalent

Physiometrix, Inc.

FDA 510(k) clearance K935260 for PHYSIOMETRIX CABLE ADAPTER MODIFICATION, Substantially Equivalent on 1993-12-23. Applicant: Physiometrix, Inc.. Device class: 2.

Clearance details

Applicant: Physiometrix, Inc.
Product code: Code IKD
Device class: Class 2
Regulation: 21 CFR 890.1175
Advisory panel: Physical Medicine
Date received: 1993-11-02
Decision date: 1993-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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