FDA 510(k) Applications for Medical Device Product Code "JQW"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K023955 | BECTON, DICKINSON & CO. | BD VIPER INSTRUMENT | 06/24/2003 |
K962859 | CAVRO SCIENTIFIC INSTRUMENTS, INC. | MINI SAMPLE PROCESSOR | 10/29/1996 |
K970616 | CAVRO SCIENTIFIC INSTRUMENTS, INC. | MINI SAMPLER PROCESSOR | 04/21/1997 |
K961896 | HAMILTON CO. | MICROLAB 4000, MICROLAB 4200 | 08/16/1996 |
K961694 | MATRIX TECHNOLOGIES CORP. | IMPACT | 06/21/1996 |
K962687 | NICHOLS INSTITUTE DIAGNOSTICS | GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM | 03/28/1997 |
K970420 | PHARMACIA, INC. | MASTERCAP AM 5.0/MASTERCAP RM 5.0 | 06/30/1997 |
K980180 | WATERS CORPORATION | 2700 SAMPLE MANAGER | 02/12/1998 |
K973335 | ZENYX SCIENTIFIC LTD. | QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE) | 04/30/1998 |