Medical Device Manufacturer · ID , Jakarta - Indonesia

Arista Latindo Industrial Ltd. P.T - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1989
21
Total
21
Cleared
0
Denied

Arista Latindo Industrial Ltd. P.T has 21 FDA 510(k) cleared general hospital devices. Based in Jakarta - Indonesia, ID.

Historical record: 21 cleared submissions from 1989 to 2004.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Arista Latindo Industrial Ltd. P.T

21 devices
1-12 of 21
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