Medical Device Manufacturer · HK , Hong Kong

Swank Plus , Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1988
3
Total
3
Cleared
0
Denied

Swank Plus , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Hong Kong, HK.

Historical record: 3 cleared submissions from 1988 to 1988. Primary specialty: Ophthalmic.

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

FDA 510(k) Regulatory Record - Swank Plus , Ltd.

3 devices
1-3 of 3
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All3 Ophthalmic 3