Airway Management, Inc. is one of 18368 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Airway Management, Inc. - FDA 510(k) Cleared Devices
Recent clearances: myTAP2, TAP 3, TAP 1, TAP PAP NASAL PILLOW MASK
6
Total
6
Cleared
0
Denied
Airway Management, Inc. has 6 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 6 cleared submissions from 2006 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Airway Management, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Promedic, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Airway Management, Inc.
6 devices
Cleared
Aug 31, 2018
myTAP2
Dental
87d
Cleared
Aug 10, 2016
TAP 3, TAP 1
Dental
191d
Cleared
Nov 01, 2012
TAP PAP NASAL PILLOW MASK
Anesthesiology
90d
Cleared
Dec 12, 2006
TAP III ANTI-SNORING DEVICE
Dental
74d
Cleared
Jul 12, 2006
TAP-T
Dental
22d
Cleared
May 17, 2006
TAP II ANTI-SNORING AND OBSTRUCTIVE SLEEP APNEA ORAL APPLIANCE WITH ATTACHMENT
Dental
92d