Sphygmetrics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K800401INFRASONDE D4000 ELECTRONIC B-P MONITORMarch 12, 1980
K800179INFRASONDE AUTO/INFLATOR ELEC. VIBRATORFebruary 11, 1980