ClearanceBrief
Company ยท US

Verimed Holdings, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1998. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HCCDevice, Biofeedback5
HIRPerineometer3
IPFStimulator, Muscle, Powered3
KQXGoniometer, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 20, 1998K981277PERIFORM
Verimed Holdings, Inc.
HIR
Nov 14, 1995K954127BIOFEEDBACK DEVICE
Verimed Holdings, Inc.
HCC
Jun 14, 1995K951969MYOEXORCISER II FUAL
Verimed Holdings, Inc.
HCC
Jul 2, 1993K930670PHYACTION 787
Verimed Holdings, Inc.
IPF
Dec 10, 1992K922550ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)
Verimed Holdings, Inc.
KQX
Jun 16, 1992K913912VERIMED PERINEOMETER
Verimed Holdings, Inc.
HIR
Mar 7, 1990K893220VERIMED MYOEXORCISER VERISTIM
Verimed Holdings, Inc.
IPF
Dec 13, 1989K892649VERIMED MYOEXORCISER III (MYO III)
Verimed Holdings, Inc.
HCC
Aug 8, 1988K874212VERIMED MYO/PREMS
Verimed Holdings, Inc.
IPF
Jun 9, 1986K854193ELECTRO-MYOGRAPHIC PERINEOMETER
Verimed Holdings, Inc.
HIR
Jan 21, 1986K852963MYO-ACTUATOR
Verimed Holdings, Inc.
HCC
Oct 28, 1983K832714VERIMED MYOEXORCISER
Verimed Holdings, Inc.
HCC

Latest recalls

DateFirm and productCodeLinked 510(k)
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