ClearanceBrief
Company ยท US

Fasstech

FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2007. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HCCDevice, Biofeedback5
IKNElectromyograph, Diagnostic3
KQXGoniometer, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 16, 2007K063447INSIGHT DISCOVERY
Fasstech
IKN
Nov 28, 2003K033452CWAS 1000
Fasstech
IKN
Oct 10, 2003K023209INSIGHT MILLENNIUM III
Fasstech
IKN
Sep 20, 2001K011964INSIGHT MILLENNIUM PLUS
Fasstech
HCC
Aug 30, 2001K011983INSIGHT GENESIS
Fasstech
HCC
Jun 3, 1999K990778INSIGHT MILLENNIUM
Fasstech
HCC
Jun 12, 1996K961212SPINAL TOUCH
Fasstech
KQX
Feb 24, 1995K940050FOCUS EMG
Fasstech
HCC
Feb 2, 1993K925197PSI 220 DUAL EMG
Fasstech
HCC

Latest recalls

DateFirm and productCodeLinked 510(k)
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