Ferno-Washington, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ferno-Washington, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Ferno-Washington, Inc. has 5 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 5 cleared submissions from 1986 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ferno-Washington, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ferno-Washington, Inc.
5 devices
Cleared
Apr 21, 1998
FERNO HEALTHCARE RECLINE-A-BATH 2
Physical Medicine
106d
Cleared
Sep 09, 1993
FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-IT
General Hospital
114d
Cleared
Dec 17, 1986
MODEL 668, TRACTION SPLINT, ADULT
Neurology
12d
Cleared
Nov 13, 1986
MODEL 35-B ALL LEVEL COT
General Hospital
15d
Cleared
Sep 12, 1986
EZ LOAD MODEL 30, ALL LEVEL COT
General Hospital
78d