Tsi, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Tsi, Inc. Cardiovascular ✕
4 devices
Cleared
Feb 13, 1990
LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2
Cardiovascular
90d
Cleared
Sep 19, 1988
MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A
Cardiovascular
277d
Cleared
Feb 20, 1987
MODIFIED LASERFLO BLOOD PERFUSION MONITOR
Cardiovascular
114d
Cleared
Jun 24, 1985
LASERFLO BLOOD PERFUSION MONITOR 403
Cardiovascular
102d