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Sontra Medical, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K040525SONOPREP ULTRASONIC SKIN PERMEATION SYSTEM AND TOPICAL ANESTHETIC KIT, MODEL D2000August 17, 2004
K023713SONOPREP IMPEDANCE DIAGNOSTICS (IDX) SYSTEM, MODEL D1000January 28, 2004