Sims Portex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HYPODERMIC NEEDLE-PRO NEEDLE WITH NEEDLE PROTECTION DEVICE, ELECTROSTATIC HYDROPHOBIC BREATHING FILTER, BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sims Portex, Inc. General Hospital ✕
4 devices
Cleared
Jul 12, 2001
HYPODERMIC NEEDLE-PRO NEEDLE WITH NEEDLE PROTECTION DEVICE
General Hospital
22d
Cleared
Feb 05, 2001
ELECTROSTATIC HYDROPHOBIC BREATHING FILTER
General Hospital
200d
Cleared
Dec 14, 2000
BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT
General Hospital
121d
Cleared
Feb 22, 2000
SIMS PORTEX ANESTHESIA CATHETER
General Hospital
64d