Medical Device Manufacturer · US , Lakewood , NJ

E.W.A., Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1992
2
Total
2
Cleared
0
Denied

E.W.A., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Lakewood, US.

Historical record: 2 cleared submissions from 1992 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by E.W.A., Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - E.W.A., Ltd.

2 devices
1-2 of 2
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