Protek Medical Products, Inc.
Protek Medical Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 1998.
Top product codes for Protek Medical Products, Inc.
Recent clearances by Protek Medical Products, Inc.
- K973958 — GENERAL PURPOSE ATL NEEDLE GUIDE KIT
- K973622 — TRANSDUCER POSITIONER
- K970889 — ULTRASOUND TRANSDUCER DRAPE
- K970893 — ULTRASOUND TRANSDUCER DRAPE
- K973362 — NEEDLE GUIDE/GRID
- K970885 — ULTRASOUND SYSTEMS DRAPE
- K970891 — DRAPE, SURGICAL-LATEX
- K971722 — TRANS VAGINAL NEEDLE GUIDE
- K971115 — GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE
Data sourced from openFDA. This site is unofficial and independent of the FDA.