Medical Device Manufacturer · US , Round Rock , TX

Kiscomedica S.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008
1
Total
1
Cleared
0
Denied

Kiscomedica S.A. has 1 FDA 510(k) cleared medical devices. Based in Round Rock, US.

Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Kiscomedica S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kiscomedica S.A.
1 devices
1-1 of 1
Cleared Jun 30, 2008
L-VARLOCK
K080537 · MAX
Orthopedic · 124d
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