ApneaLink Air— 510(k) K143272

Substantially Equivalent

Resmed Germany, Inc.

FDA 510(k) clearance K143272 for ApneaLink Air, Substantially Equivalent on 2015-04-30. Applicant: Resmed Germany, Inc.. Device class: 2.

Clearance details

Applicant
Resmed Germany, Inc.
Product code
Code MNR
Device class
Class 2
Regulation
21 CFR 868.2375
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Martinsried, DE
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