Medical Device Manufacturer · US , Chester , NJ

P.T. Latexindo Prautama - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1989
3
Total
3
Cleared
0
Denied

P.T. Latexindo Prautama has 3 FDA 510(k) cleared medical devices. Based in Chester, US.

Historical record: 3 cleared submissions from 1989 to 1991. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by P.T. Latexindo Prautama Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - P.T. Latexindo Prautama

3 devices
1-3 of 3
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