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FDA 510(k) Applications for Medical Device Product Code "BXX"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K791294 | EQUILIBRATED BIO SYSTEMS, INC. | SPIROCAL | 08/16/1979 |
K923397 | ESCALON MEDICAL TREK | SINGLE DOSE GAS INJECTOR | 09/14/1992 |
K801256 | KLEEN TEST PRODUCTS | NEEDLE COUNTER-SURE COUNT-DISPOSA-TRAY | 06/04/1980 |
K801258 | KLEEN TEST PRODUCTS | NEEDLE COUNTER-SURE COUNT/10 COUNT | 06/04/1980 |
K801257 | KLEEN TEST PRODUCTS | NEEDLE COUNTER-SURE COUNT/30 CT. MAGN. | 06/04/1980 |
K780838 | MICRO TRONICS CORP. | PERCI | 07/17/1978 |
K780981 | PENNWALT CORP. | PORTABLE PNEUMATIC CALIBRATOR 65-150 | 08/02/1978 |
K822746 | TIMETER INSTRUMENT CORP. | RT-200 CALIBRATION ANALYZER | 10/13/1982 |
K875075 | TIMETER INSTRUMENT CORP. | RT-200 COMPUTER INTERFACE | 04/21/1988 |
K850029 | UTAH MEDICAL PRODUCTS, INC. | UTAH PRESSURE TRANSDUCER CALIBRATOR TRU-CAL | 04/29/1985 |