NEUROCOM PRESSURE TEST SYSTEM— 510(k) K871652

Name: FDA 510(k) clearance K871652
Creator: U.S. Food and Drug Administration
Published: 1987-07-16

Substantially Equivalent

Neurocom International, Inc.

FDA 510(k) clearance K871652 for NEUROCOM PRESSURE TEST SYSTEM, Substantially Equivalent on 1987-07-16. Applicant: Neurocom International, Inc.. Device class: 2.

Clearance details

Applicant: Neurocom International, Inc.
Product code: Code ETY
Device class: Class 2
Regulation: 21 CFR 874.1090
Advisory panel: Ear, Nose, Throat
Date received: 1987-04-28
Decision date: 1987-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clackamas, OR, US

Download summary PDF View on FDA.gov ↗

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