FDA 510(k) Applications Submitted by KOROS USA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120590 | 02/28/2012 | DILATOR TUBE SET | KOROS USA, INC. |
| K071338 | 05/14/2007 | FLEX ARM RETRACTOR SYSTEM | KOROS USA, INC. |
| K101609 | 06/08/2010 | SELF RETAINING SOFT TISSUE RETRACTOR | KOROS USA, INC. |
| K082399 | 08/20/2008 | PECTUS STRUT | KOROS USA, INC. |
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