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Sphygmetrics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K800401
INFRASONDE D4000 ELECTRONIC B-P MONITOR
March 12, 1980
K800179
INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR
February 11, 1980