Medical Device Manufacturer · CH , Horgen, Switzerland

Max Staubli , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986
1
Total
1
Cleared
0
Denied

Max Staubli , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Horgen, Switzerland, CH.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Max Staubli , Ltd.

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