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Pentapharm GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K083842ROTEM DELTA THROMBOELASTOMETRY SYSTEMMarch 23, 2010
K042762PEFAKIT APC-R FACTOR V LEIDENDecember 22, 2004
K042760PEFAKIT APC-R FACTOR V LEIDEN CONTROLSDecember 22, 2004