FDA 510(k) Applications for Medical Device Product Code "LBB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K042889 | AMETEK | DYNAMOMETER - MODEL FCE AND MODEL MSC | 11/16/2004 |
K073154 | GLOBAL SERVICES GROUP, LLC | FACTS HAND AND PINCH GRIP COMBO | 02/14/2008 |
K162412 | Hoggan Scientific, LLC | Hoggan Scientific« microFET2Ö | 03/09/2017 |
K964685 | JOHN CHATILLON & SONS, INC. | DYNAMOMETER | 01/27/1997 |
K012492 | KADA RESEARCH, INC. | KADANCE 2000 | 11/02/2001 |
K964933 | MEKANIKA, INC. | MEKANIKA'S SPINAL STIFFNESS GAUGE (SSG) | 02/03/1997 |
K981730 | NK BIOTECHNICAL CORP. | DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002 | 07/17/1998 |
K980363 | OROFACIAL DYNAMICS | ORO-FACIAL MYOGRAPHIC MEASUREMENT INSTRUMENT (OMMI) | 04/16/1998 |
K052309 | SAEHAN CORP. | DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006 | 09/27/2005 |