Medical Device Manufacturer · US , Mchenry , IL

Burroughs Wellcome Co. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1977

Total

Cleared

Denied

Burroughs Wellcome Co. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 17 cleared submissions from 1977 to 1982.

Browse the FDA 510(k) cleared devices submitted by Burroughs Wellcome Co. Filter by specialty or product code using the sidebar.

Burroughs Wellcome Co. 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 - Burroughs Wellcome Co.

17 devices

1-17 of 17

DAC-CEL DIGOXIN RADIOIMMUNOASSAY KIT

FLUORESCENT ANTI. ANTI-HUMAN C3

K771583 · DAC

Microbiology · 15d

Cleared Aug 25, 1977

AGGLUTINATING SERUM W135

Burroughs Wellcome Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Burroughs Wellcome Co.

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