FDA 510(k) Applications for Medical Device Product Code "HQR"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K972749 | C.M. CHANCE LTD. | PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S) | 03/13/1998 |
K955158 | ELLMAN INTL., INC. | SURGITRON | 02/09/1996 |
K952569 | GAMP & ASSOC. | GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR | 01/05/1996 |
K990064 | OPHTHALMIC TECHNOLOGIES, INC. | DI-RHEX OPHTHALMIC DIATHERMY SYSTEM | 04/04/1999 |
K980522 | REFRACTEC, INC. | REFRACTEC MCS-100 | 07/22/1998 |
K050308 | STARION INSTRUMENTS | THERMAL CAUTERY PROBE | 02/25/2005 |
K952151 | STORZ | STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204) | 03/04/1996 |