Medical Device Manufacturer · US , Boca Raton , FL

K-Lok, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - K-Lok, Inc. General Hospital ✕

2 devices

1-2 of 2

Cleared Feb 18, 1994

K-LOK CATHETER SECUREMENT DEVICE MODIFICATION

General Hospital · 134d

Cleared Apr 21, 1993

K-LOK CATHETER SECUREMENT DEVICE

General Hospital · 96d