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FDA 510(k) Applications for Medical Device Product Code "EBA"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K854646 | ALPINE DENTAL EQUIPMENT CO. | VEGA DENTAL OPERATING LIGHT | 03/06/1986 |
K810117 | COLMED, LTD. | HALOGEN HEADLIGHT SYSTEM | 02/10/1981 |
K893458 | CUDA PRODUCTS CO. | FIBEROPTIC HEADLIGHT SYSTEM | 06/22/1989 |
K842515 | GOOD-LITE CO. | SURGICAL HEADLIGHT | 08/02/1984 |
K790807 | HARRY J. BOSWORTH CO. | METALIT | 08/03/1979 |
K790806 | HARRY J. BOSWORTH CO. | PORCELIT | 08/03/1979 |
K822265 | KELLEHER CORP. | FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS | 09/28/1982 |
K070287 | PHOTONIC OPTISCHE GERATE GMBH & COKG | PS SERIES WITH FIBER LIGHT GUIDE AND HEADLIGHT, MODELS PS200, PS250, PS500 | 02/12/2007 |
K842358 | PLANMECA USA, INC. | ISOLIGHT | 07/31/1984 |
K923949 | SYLVAN MEDICAL FIBEROPTICS | SYLVAN DENTAL HEADLIGHT SYSTEM | 10/16/1992 |