Medical Device Manufacturer · US , Libertyville , IL

Maika Rubber Products Sdn Bhd - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998
1
Total
1
Cleared
0
Denied

Maika Rubber Products Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Libertyville, US.

Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Maika Rubber Products Sdn Bhd Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Maika Rubber Products Sdn Bhd

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