APNEALINK PRO— 510(k) K131932

Substantially Equivalent

Resmed Germany, Inc.

FDA 510(k) clearance K131932 for APNEALINK PRO, Substantially Equivalent on 2013-11-08. Applicant: Resmed Germany, Inc..

Clearance details

Applicant: Resmed Germany, Inc.
Product code: Code MNR
Advisory panel: Anesthesiology
Date received: 2013-06-27
Decision date: 2013-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Martinsried, DE

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.