Portex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER, PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT, 1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
20
Total
20
Cleared
0
Denied
FDA 510(k) Regulatory Record - Portex, Inc. General Hospital ✕
2 devices