Valley Forge Scientific Corp. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Valley Forge Scientific Corp. has 27 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1980 to 2005.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Valley Forge Scientific Corp.
27 devices
Cleared
Mar 09, 2005
MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM
General & Plastic Surgery
23d
Cleared
Oct 22, 2004
VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED...
General & Plastic Surgery
28d
Cleared
Apr 01, 2004
STRYKER INTERVENTIONAL PAIN RF GENERATOR
Neurology
220d
Cleared
Nov 28, 2003
MALIS IRRIGATION MODULE 1000
General & Plastic Surgery
23d
Cleared
Aug 13, 1998
BI-DENT
Dental
90d
Cleared
Dec 19, 1997
VALLEY FORGE BIPOLAR BALL TIP ELECTRODE
General & Plastic Surgery
91d
Cleared
Aug 26, 1997
VALLEY FORGE BIPOLAR LOOP
Obstetrics & Gynecology
89d
Cleared
Jan 09, 1997
MINI-SYMM BIPOLAR COAGULATOR
General & Plastic Surgery
84d
Cleared
Mar 01, 1996
VALLEY FORGE BIPLOAR LOOP
General & Plastic Surgery
72d
Cleared
Dec 08, 1995
VFS - 300 BIPOLAR ELECTROSURGERY SYSTEM
General & Plastic Surgery
17d
Cleared
May 23, 1995
PRECISION BIPOLAR COAGULATOR
General & Plastic Surgery
26d
Cleared
Mar 11, 1993
AID, CARDIOPULMONARY RESUSCITATION
Anesthesiology
44d