W.E. Leder Enterprises, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - W.E. Leder Enterprises, Inc. Anesthesiology ✕
5 devices
Cleared
Nov 03, 1983
ARF 850 E
Anesthesiology
143d
Cleared
Sep 29, 1983
LARYNGESCOPE
Anesthesiology
101d
Cleared
Mar 09, 1983
ANESTHESIA APPARATUS PH-35
Anesthesiology
55d
Cleared
Mar 09, 1983
ANESTHESIA APPARATUS #FO 20S
Anesthesiology
55d
Cleared
Mar 09, 1983
ANESTHESIA APATATUS #D-25
Anesthesiology
55d