FDA 510(k) Applications Submitted by CATHY PETERS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090413 | 02/18/2009 | A1CNOW+ (10 TEST KIT, PROFESSIONAL USE) MODEL 3024, A1CNOW+(20 TEST KIT, PROFESSIONAL USE) MODEL 3021, A1CNOW SELF CHEC | BAYER HEALTHCARE, LLC |
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