Ipax, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
FDA 510(k) cleared devices by Ipax, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Feb 12, 1992
SUREBREATH DOME, E-Z BREATHER
General & Plastic Surgery
90d
Cleared
Oct 07, 1988
SUREBREATH DOME
General & Plastic Surgery
10d
Cleared
Sep 04, 1987
PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKS
General & Plastic Surgery
39d
Cleared
Jul 08, 1986
CATALOG NO. I/A 100 AND KPE 200
General & Plastic Surgery
28d