MODEL 9000 RECORDING SYSTEM/RESPIRATION MONITORING— 510(k) K860455

Name: FDA 510(k) clearance K860455
Creator: U.S. Food and Drug Administration
Published: 1986-04-01

Substantially Equivalent

Oxford Medilog, Inc.

FDA 510(k) clearance K860455 for MODEL 9000 RECORDING SYSTEM/RESPIRATION MONITORING, Substantially Equivalent on 1986-04-01. Applicant: Oxford Medilog, Inc.. Device class: 2.

Clearance details

Applicant: Oxford Medilog, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1986-02-05
Decision date: 1986-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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