Valley Forge Scientific Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMMarch 9, 2005
K042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSOctober 22, 2004
K032601STRYKER INTERVENTIONAL PAIN RF GENERATORApril 1, 2004
K033499MALIS IRRIGATION MODULE 1000November 28, 2003
K982229BI-DENTAugust 13, 1998
K973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODEDecember 19, 1997
K971986VALLEY FORGE BIPOLAR LOOPAugust 26, 1997
K964143MINI-SYMM BIPOLAR COAGULATORJanuary 9, 1997
K955764VALLEY FORGE BIPLOAR LOOPMarch 1, 1996
K955346VFS - 300 BIPOLAR ELECTROSURGERY SYSTEMDecember 8, 1995
K951985PRECISION BIPOLAR COAGULATORMay 23, 1995
K930429AID, CARDIOPULMONARY RESUSCITATIONMarch 11, 1993
K923928BIPOLAR COAGULATOR/IRRIAGATION SYSTEMJanuary 22, 1993
K924188BI-TECH I BIPOLAR COAGULATOR/CUTTING SYSTEMDecember 10, 1992
K910510VALLEY FORGE BIPOLAR PEN OR FORCEPSApril 22, 1991
K896541MALIS BIPOLAR ELECTROSURGICAL SYSTEM CMC-IIIJanuary 29, 1990
K890648MALIS BIPOLAR CORD/IRRIGATION TUBING SETMarch 3, 1989
K890309MALIS SURGICAL STOOLFebruary 14, 1989
K874845MALIS SURGICAL LOUPESDecember 23, 1987
K861822MALIS SURGICAL MESH FOR SKULL /SPINAL COLUMN REPAIJuly 11, 1986