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Pulse Scientific, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K923768
PULSE CRP TEST
December 1, 1992
K923767
PULSE IM RED CELL TEST
October 16, 1992
K923771
PULSE RF TEST
October 5, 1992