FDA 510(k) Applications Submitted by GDS TECHNOLOGY, LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K971145 03/28/1997 GLUCOSITE TEST SYSTEM GDS TECHNOLOGY, LLC.
K973649 09/25/1997 HEMOSITE TEST SYSTEM GDS TECHNOLOGY, LLC.
K992132 06/23/1999 CHOLESITE TEST SYSTEM GDS TECHNOLOGY, LLC.
K994073 12/02/1999 HEMOSITE TEST SYSTEM GDS TECHNOLOGY, LLC.


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