Medical Device Manufacturer · SE , Stockholm

Medtronic-Synectics - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Medtronic-Synectics has 1 FDA 510(k) cleared medical devices. Based in Stockholm, SE.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Medtronic-Synectics Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic-Synectics

1 devices

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