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Danmar Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
6
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K090341MICHIGAN CRANIAL RESHAPING ORTHOSISJanuary 6, 2010
K013452DANMAR PRODUCTS CRANIAL ADJUSTIVE PROSTHESISOctober 31, 2003
K003630DANMAR PRODUCTS MICHIGAN CRANIAL HELMETMay 29, 2001