Medical Device Manufacturer · ZA , Cape Town, Western Cape

Iqteq Development - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Iqteq Development has 1 FDA 510(k) cleared medical devices. Based in Cape Town, Western Cape, ZA.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Iqteq Development Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Iqteq Development

1 devices

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