FDA 510(k) Applications Submitted by INVERNESS MEDICAL PROFESSIONAL DIAGNOSTICS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070522 | 02/23/2007 | MODIFICATION TO: BINAX NOW LEGIONELLA URINARY ANTIGEN TEST, #852-000,852-012 | INVERNESS MEDICAL PROFESSIONAL DIAGNOSTICS |
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