Medical Device Recalls
-
|
1 result found
510(K) Number: K031399 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: DBM002, DBM005, DBM010,... | 3 | 02/14/2008 |
FEI # 1000160576 Interpore Cross International Inc |
-







