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FDA 510(k) Applications for Medical Device Product Code "MIC"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K021337 | AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. | AART PECTORALIS IMPLANT | 07/03/2002 |
K973729 | HANSON MEDICAL, INC. | POWERFLEX PEC IMPLANT | 12/24/1997 |
K002633 | PILLAR SURGICAL, INC. | SILMAX PECTORAL IMPLANT | 11/21/2000 |
K961072 | RAND SCIENTIFIC CORP. | PEC IMPLANT | 04/19/1996 |
K982762 | SEARE BIOMEDICAL CORP. | SEARE BIOMEDICAL PECTORALIS IMPLANT | 09/30/1998 |
K983043 | SEARE BIOMEDICAL CORP. | SEARE BIOMEDICAL SILICONE BLOCK | 09/30/1998 |