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FDA 510(k) Applications for Medical Device Product Code "HQO"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K962135 | DUTCH OPHTHALMIC USA, INC. | D.O.R.C. MICRODIATHERMY SYSTEM | 08/29/1996 |
K002341 | GEIGER MEDICAL TECHNOLOGIES, INC. | THERMAL CAUTERY UNIT, MODEL 150 | 10/23/2000 |
K971538 | MENTOR OPHTHALMICS, INC. | MENTOR GEMINI HEMOSTATIC ERASER | 07/14/1997 |
K000893 | STARION INSTRUMENTS | AC POWERED THERMAL CAUTERY UNIT | 06/14/2000 |
K070871 | STARION INSTRUMENTS | STARION UNIVERSAL POWER SUPPLY | 04/13/2007 |
K043155 | STARION INSTRUMENTS | STARION UNIVERSAL POWER SUPPLY (UPS) | 12/09/2004 |