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Revivant Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040453AUTOPULSE RESUSCITATION SYSTEM, MODEL 100March 11, 2004
K032852MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100November 12, 2003
K022345AUTOPULSE RESUSCITATION SYSTEMAugust 15, 2002
K011046AUTOPULSE, MODEL 100October 25, 2001