APNEALINK, MODEL 22302— 510(k) K061405

Substantially Equivalent

Resmed Germany, Inc.

FDA 510(k) clearance K061405 for APNEALINK, MODEL 22302, Substantially Equivalent on 2006-07-25. Applicant: Resmed Germany, Inc..

Clearance details

Applicant: Resmed Germany, Inc.
Product code: Code MNR
Advisory panel: Anesthesiology
Date received: 2006-05-19
Decision date: 2006-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Poway, CA, US

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