MEDILOG VISION— 510(k) K961636

Substantially Equivalent

Oxford Instruments, Plc.

FDA 510(k) clearance K961636 for MEDILOG VISION, Substantially Equivalent on 1997-01-17. Applicant: Oxford Instruments, Plc.. Device class: 2.

Clearance details

Applicant: Oxford Instruments, Plc.
Product code: Code OLZ
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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Data sourced from openFDA. This site is unofficial and independent of the FDA.