Medical Device Manufacturer · US , Centerville , OH

Micro Tek Engineering - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988
2
Total
2
Cleared
0
Denied

Micro Tek Engineering has 2 FDA 510(k) cleared medical devices. Based in Centerville, US.

Historical record: 2 cleared submissions from 1988 to 1988. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Micro Tek Engineering Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Micro Tek Engineering
2 devices
1-2 of 2
Cleared Mar 29, 1988
THUMPER MODEL P-1000
K880597 · BYI
Anesthesiology · 47d
Cleared Feb 10, 1988
THERMAL-PAK MODEL SW 1000
K880252 · LHC
General Hospital · 21d
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All2 General Hospital 1 Anesthesiology 1