Medical Device Manufacturer · IT , Porto Mantovano, Mn

Modissa 90 Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993
2
Total
2
Cleared
0
Denied

Modissa 90 Srl has 2 FDA 510(k) cleared medical devices. Based in Porto Mantovano, Mn, IT.

Historical record: 2 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Modissa 90 Srl Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Modissa 90 Srl

2 devices
1-2 of 2
Cleared Oct 20, 1993
MODISSA 90 S.R.L. SUNGLASSES
K930858 · HQY
Ophthalmic · 244d
Cleared Aug 25, 1993
MODISSA 90 S.R.L. SPECTACLE FRAMES
K930857 · HQZ
Ophthalmic · 188d
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