ClearanceBrief
Company ยท US

J-Tech, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1996. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KQXGoniometer, Ac-Powered2
FJLResectoscope1
HCCDevice, Biofeedback1
LBBDynamometer, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 3, 1996K954737SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICE
J-Tech, Inc.
HCC
Oct 30, 1995K954647INCLINOMETER
J-Tech, Inc.
KQX
May 10, 1995K945630LARGE MUSCLE STRENGTH GAUGE
J-Tech, Inc.
KQX
Oct 23, 1991K913587JTECH 50 SERIES CUTTING LOOP
J-Tech, Inc.
FJL
Sep 5, 1991K912526GS-220 HAND IMPAIRMENT EVALUATION SYSTEM
J-Tech, Inc.
LBB

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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