MEDILOG MPA-S— 510(k) K961638

Name: FDA 510(k) clearance K961638
Creator: U.S. Food and Drug Administration
Published: 1997-01-17

Substantially Equivalent

Oxford Instruments Medical Systems

FDA 510(k) clearance K961638 for MEDILOG MPA-S, Substantially Equivalent on 1997-01-17. Applicant: Oxford Instruments Medical Systems. Device class: 2.

Clearance details

Applicant: Oxford Instruments Medical Systems
Product code: Code OLV
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1996-04-29
Decision date: 1997-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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