Medisiss
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113028 | MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS | HRX | 2011-12-20 | View |
| 510(k) | K100543 | MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01 | GEI | 2010-07-23 | View |
| 510(k) | K081559 | GENESIS | GEI | 2008-08-28 | View |
| 510(k) | K042659 | MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS | NON | 2005-02-14 | View |
| 510(k) | K030598 | MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS | NLQ | 2004-01-23 | View |
| 510(k) | K030919 | SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES | NLR | 2003-07-03 | View |
No matching devices.
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