MEDILOG OPTIMA— 510(k) K896535

Substantially Equivalent

Oxford Medilog, Inc.

FDA 510(k) clearance K896535 for MEDILOG OPTIMA, Substantially Equivalent on 1990-01-18. Applicant: Oxford Medilog, Inc.. Device class: 2.

Clearance details

Applicant: Oxford Medilog, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1989-11-14
Decision date: 1990-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Oxford Medilog, Inc.

K923737 — MODEL MEDILOG RAPIDE1994-01-05
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K912639 — SONICAID TEAM1991-12-31
K904763 — MENTOR EEG SYSTEM1991-04-10

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