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Versamed , Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K021981IVENT 201 PORTABLE VENTILATORAugust 13, 2003
K011957IVENT 201 PORTABLE VENTILATORJuly 18, 2001
K981668SMARTVENT 201 PORTABLE VENTILATORApril 7, 1999