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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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