Stephenson Industries, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Stephenson Industries, Inc. has 4 FDA 510(k) cleared medical devices. Based in Farmingdale, US.
Historical record: 4 cleared submissions from 1985 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stephenson Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stephenson Industries, Inc.
4 devices
Cleared
Jul 28, 1997
HYPER PULSE INTERMITTENT TOPICAL OXYGEN CHAMBER C-100, CB-100
General & Plastic Surgery
311d
Cleared
May 12, 1986
TOPICAL HYPERBARIC OXYGEN CHAMBER
General & Plastic Surgery
13d
Cleared
May 06, 1986
THE NEW FLEXIBLE COLLAPSIBLE CHAMBER
General & Plastic Surgery
43d
Cleared
Dec 09, 1985
REGULATOR-INHALATOR SYSTEM
Anesthesiology
74d