Medical Device Manufacturer · US , Denver , CO

Transtracheal Systems - FDA 510(k) Cleared Devices

8 submissions · 7 cleared · Since 1986

Recent clearances: TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000, TRANSTRACHEAL AUGMENTED VENTILATION OXYGEN CONCENTRATOR MODEL NUMBER TTAV 1000, SCOOP 1

8

Total

7

Cleared

0

Denied

Transtracheal Systems has 7 FDA 510(k) cleared medical devices. Based in Denver, US.

Historical record: 7 cleared submissions from 1986 to 1999. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Transtracheal Systems Filter by specialty or product code using the sidebar.

Transtracheal Systems is one of 7868 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Transtracheal Systems

8 devices

1-8 of 8

Cleared Jul 12, 1999

TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000

Anesthesiology · 325d

Cleared Jul 23, 1998

TRANSTRACHEAL AUGMENTED VENTILATION OXYGEN CONCENTRATOR MODEL NUMBER TTAV 1000

Anesthesiology · 121d

Cleared Jun 17, 1998

Anesthesiology · 85d

Cleared Oct 23, 1996

TRANSTRACHEAL DEMAND OXYGEN CONTROLLER (DOC-2000)

Anesthesiology · 89d

Cleared Mar 01, 1991

TRANSKINETICS INFRARED MULTI-LEAD TELE SYST 7100

Cardiovascular · 133d

Cleared Mar 01, 1991

TRANSKINETICS RADO FREQ MULTI-LEAD TELE SYST 7200

Cardiovascular · 133d

Cleared Aug 10, 1990

MODIFIED SCOOP TRANSTRACHEAL CATHETERS

Anesthesiology · 80d

Cleared Feb 03, 1986

TRANSTRACHEAL SYSTEM-SCOOP-INSERTION TRAY-CATHETER

Anesthesiology · 104d