FDA 510(k) Applications Submitted by MELODY BI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132357 | 07/29/2013 | SMITH & NEPHEW ULTRATAPE | SMITH & NEPHEW, INC. |
| K102737 | 09/22/2010 | KENDALL SCD 700 SEQUENTIAL COMPRESSION CONTROLLER | Covidien LLC |
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