MODEL 9000 RECORDING & ELECTROPHYSIOLOGICAL SYSTEM— 510(k) K860456

Substantially Equivalent

Oxford Medilog, Inc.

FDA 510(k) clearance K860456 for MODEL 9000 RECORDING & ELECTROPHYSIOLOGICAL SYSTEM, Substantially Equivalent on 1986-08-11. Applicant: Oxford Medilog, Inc.. Device class: 2.

Clearance details

Applicant
Oxford Medilog, Inc.
Product code
Code GWQ
Device class
Class 2
Regulation
21 CFR 882.1400
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Clearwater, FL, US
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