FDA 510(k) Applications Submitted by ITL CORPORATION, PTY LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000777 | 03/09/2000 | SAMPLOK | ITL CORPORATION, PTY LTD. |
| K991404 | 04/22/1999 | PLATYPUS AV FISTULA NEEDLE PROTECTOR (AVFNP) | ITL CORPORATION, PTY LTD. |
| K021941 | 06/13/2002 | SAMPLOK LUER KIT | ITL CORPORATION, PTY LTD. |
| K021017 | 03/29/2002 | LEESPEC DISPOSABLE VAGINAL SPECULUM | ITL CORPORATION, PTY LTD. |
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