Medical Device Manufacturer · US , Mchenry , IL

Merck, Sharp & Dohme - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1976

Total

Cleared

Denied

Merck, Sharp & Dohme has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1976 to 1988. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Merck, Sharp & Dohme Filter by specialty or product code using the sidebar.

Merck, Sharp & Dohme is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Merck, Sharp & Dohme

4 devices

1-4 of 4