Sontra Medical, Inc. is one of 25727 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sontra Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SONOPREP ULTRASONIC SKIN PERMEATION SYSTEM AND TOPICAL ANESTHETIC KIT, MODEL D2000, SONOPREP IMPEDANCE DIAGNOSTICS (IDX) SYSTEM, MODEL D1000
2
Total
1
Cleared
0
Denied
Sontra Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sontra Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sontra Medical, Inc.
2 devices