Verimed Holdings, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K981277PERIFORMNovember 20, 1998
K954127BIOFEEDBACK DEVICENovember 14, 1995
K951969MYOEXORCISER II FUALJune 14, 1995
K930670PHYACTION 787July 2, 1993
K922550ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)December 10, 1992
K913912VERIMED PERINEOMETERJune 16, 1992
K893220VERIMED MYOEXORCISER VERISTIMMarch 7, 1990
K892649VERIMED MYOEXORCISER III (MYO III)December 13, 1989
K874212VERIMED MYO/PREMSAugust 8, 1988
K854193ELECTRO-MYOGRAPHIC PERINEOMETERJune 9, 1986
K852963MYO-ACTUATORJanuary 21, 1986
K832714VERIMED MYOEXORCISEROctober 28, 1983