Medical Device Manufacturer · US , Caledonia , WI

Vaughan Weeks - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

Vaughan Weeks has 2 FDA 510(k) cleared medical devices. Based in Caledonia, US.

Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Vaughan Weeks Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vaughan Weeks

2 devices
1-2 of 2
Cleared Nov 18, 1997
SYNTEC TRUE LIGHT END IRRIGATING ENDOILLUMINATOR
K973293 · MPA
Ophthalmic · 77d
Cleared Nov 14, 1997
SYNTEC TRUE LIGHT ENDOILLUMIINATOR WITH PICK
K973290 · MPA
Ophthalmic · 73d
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