Koros USA, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120590 | DILATOR TUBE SET | PDQ | 2013-05-07 | View |
| 510(k) | K101609 | SELF RETAINING SOFT TISSUE RETRACTOR | LXH | 2010-12-09 | View |
| 510(k) | K082399 | PECTUS STRUT | HRS | 2009-11-05 | View |
| 510(k) | K071338 | FLEX ARM RETRACTOR SYSTEM | GZT | 2007-05-29 | View |
No matching devices.
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