FDA 510(k) Applications for Medical Device Product Code "GAA"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K102274 | ARVIK ENTERPRISES/ MINI LAP TECHNOLOGIES | ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT | 06/15/2011 |
K011586 | DIAMETRICS MEDICAL, INC. | IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGE | 11/16/2001 |
K974741 | MEDICAL DEVICE TECHNOLOGIES, INC. | MANAN ACCURA NEEDLE | 01/08/1998 |
K961959 | MEDICAL DEVICE TECHNOLOGIES, INC. | MD TECH BIOPSY SET FOR BONE AND BONE MARROW | 07/19/1996 |
K223625 | Pneumeric, Inc. | CapnoSpotÖ Pneumothorax Decompression Indicator | 03/28/2023 |
K962425 | RADI MEDICAL SYSTEMS AB | BONOPTY COAXIAL BONE BIOPSY SYSTEM WITH ECCENTRIC DRILL(10-1072,3,4) | 09/11/1996 |
K983200 | XIMED/PROSURE/INJECTX | INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX | 12/11/1998 |
K994151 | XIMED/PROSURE/INJECTX | PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES | 03/01/2000 |