FDA 510(k) Applications Submitted by LAURUS MEDICAL CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960317 | 01/23/1996 | LAURUS NEEDLE CORE BIOPSY SYSTEM | LAURUS MEDICAL CORP. |
| K973215 | 08/27/1997 | STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM | LAURUS MEDICAL CORP. |
| K973415 | 09/09/1997 | CURVILINEAR SUTURE PLACEMENT SYSTEM | LAURUS MEDICAL CORP. |
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