FDA 510(k) Applications Submitted by AUREX SA (PTY) LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K001477 05/11/2000 AURELUX Y 84 PREMIUM AUREX SA (PTY) LTD.
K001478 05/11/2000 AURECAST SUPER INLAY AUREX SA (PTY) LTD.
K001479 05/11/2000 PALCERAM 53 AUREX SA (PTY) LTD.
K001480 05/11/2000 AURECAST 40 B AUREX SA (PTY) LTD.
K001481 05/11/2000 PALCERAM 49 AUREX SA (PTY) LTD.
K001482 05/11/2000 AURENORM 75 KF AUREX SA (PTY) LTD.


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