FDA 510(k) Applications Submitted by RETO KUETTEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K063814 | 12/22/2006 | BP-200 PLUS | SCHILLER AG |
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FDA 510(k) Applications Submitted by RETO KUETTEL
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Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact |
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