Medical Device Manufacturer · US , Mchenry , IL

Sybron Corp. - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 1977

37

Total

37

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sybron Corp. Cardiovascular ✕

3 devices

1-3 of 3

Cleared May 21, 1984

TYCOS SELF CHECK BPM3 BLOOD PRESS MONI

Cardiovascular · 108d

Cleared Nov 14, 1983

DIGITAL INJECTOR SYS

Cardiovascular · 61d

Cleared Mar 01, 1982

TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER

Cardiovascular · 42d