FDA 510(k) Applications for Medical Device Product Code "NYN"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K052625 | BIONICARE MEDICAL TECHNOLOGIES, INC. | BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000 | 12/05/2005 |
K030332 | BIONICARE MEDICAL TECHNOLOGIES, INC. | MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000 | 06/06/2003 |
K983228 | MURRAY ELECTRONICS | BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000 | 03/15/1999 |
K971437 | MURRAY ELECTRONICS | BIONICARE STIMULATOR SYSTEM. MODEL BIO-1000 | 07/22/1997 |
K073386 | PAIN MANAGEMENT TECHNOLOGIES | JOINT STIM, MODEL 1000 | 07/30/2008 |
K062325 | RS MEDICAL | RS-4I MUSCLE STIMULATOR FAMILY | 04/13/2007 |
K111557 | SEVEN SEAS DISTRIBTION AND MANUFACTURING LLC | X-FORCE | 11/10/2011 |
K142236 | VISION QUEST INDUSTRIES, INC. | BioniCare Hand System | 03/23/2015 |