Medical Device Manufacturer · GB , Guildford, Surrey England

Mercia Diagnostics , Ltd. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1987

Total

Cleared

Denied

Mercia Diagnostics , Ltd. has 17 FDA 510(k) cleared microbiology devices. Based in Guildford, Surrey England, GB.

Historical record: 17 cleared submissions from 1987 to 1992.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Mercia Diagnostics , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mercia Diagnostics , Ltd.

17 devices

1-12 of 17

CAPTIA(R) SYPHILIS M, MODIFICATION

K904524 · LIP

Microbiology · 90d

Cleared Mar 08, 1990

MODIFIED CAPTIA(R) SYPHILIS-M

MODIFIED CAPTIA(R) TOXO-M

Mercia Diagnostics , Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mercia Diagnostics , Ltd.

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