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Synthemed Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K082276SYNTHEMED DEVICENovember 18, 2008
K812464SYNTHEMED PULSE GENERATOR VVI MODEL 1000November 16, 1981