Emerald Medical, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Emerald Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 4 cleared submissions from 1996 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Emerald Medical, Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Mar 06, 2003
SYNTHETICARE POWDER-FREE VINYL EXAMINATION GLOVES
General Hospital
20d
Cleared
Mar 06, 2003
SYNTHETICARE POWDERED VINYL EXAMINATION GLOVES
General Hospital
20d
Cleared
Jan 28, 1997
EMERALD MEDICAL, INC. NUCLEUS PULPOSIS EVACUATOR SYSTEM
Orthopedic
50d
Cleared
May 28, 1996
EMERALD STERILE GAUZE SPONGE
General & Plastic Surgery
34d