FDA 510(k) Applications Submitted by OSTEX INTL., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K980518 01/16/1998 OSTEOMARK OSTEX INTL., INC.
K961562 04/22/1996 OSTEOMARK OSTEX INTL., INC.
K983457 09/30/1998 OSTEOMARK NTX SERUM EIA OSTEX INTL., INC.
K011052 04/06/2001 OSTEOMARK NTX POINT OF CARE PRESCRIPTION HOME USE OSTEX INTL., INC.


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