Medical Device Manufacturer · US , Lenexa , KS

Dyna-Tek Industries - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991
2
Total
2
Cleared
0
Denied

Dyna-Tek Industries has 2 FDA 510(k) cleared medical devices. Based in Lenexa, US.

Historical record: 2 cleared submissions from 1991 to 1997. Primary specialty: Toxicology.

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

FDA 510(k) Regulatory Record - Dyna-Tek Industries

2 devices
1-2 of 2
Cleared Feb 04, 1997
DE-TOX CONTROL 1 AND DE-TOX CONTROL 19
K964771 · DIF
Toxicology · 69d
Cleared Jan 17, 1991
DE-TOX TUBES A AND DE-TOX TUBES B
K904326 · DPA
Toxicology · 119d
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