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FDA 510(k) Applications for Medical Device Product Code "GLQ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K101335 | Streck | CELL-CHEX | 08/23/2010 |
K110718 | Streck | CELL-CHEX WITH CPPD CRYSTALS | 05/26/2011 |
K111211 | Streck | CELL-DYN 22 PLUS CONTROL | 12/22/2011 |
K090137 | Streck | STAK-CHEX PLUS RETICS | 03/18/2009 |
K000945 | STRECK LABORATORIES, INC. | PARA 12 PLUS RETICS | 04/18/2000 |
K992887 | STRECK LABORATORIES, INC. | STAK-CHEX PLUS RETICS | 11/22/1999 |
K994388 | STRECK LABORATORIES, INC. | XE CHECK | 01/14/2000 |