510(k) K182292

VORTRAN APM-Plus by Vortran Medical Technology 1, Inc. — Product Code CAP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 2019
Date Received
August 23, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
Device Class
Class II
Regulation Number
868.2600
Review Panel
AN
Submission Type