Medical Device Manufacturer · US , Jeffrey , NH

Teleflex, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1986

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Teleflex, Inc. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Feb 21, 2013

PERCUTANEOUS INTRODUCER KIT

Cardiovascular · 57d

Cleared Jun 19, 1986

MODIFIED TELEFLEX MEDICAL INTRODUCER CATHETER

Cardiovascular · 30d

Cleared May 20, 1986

PEEL AWAY & SPLIT SHEATH PERCU CATH INTRODUCER SET

Cardiovascular · 112d