FDA 510(k) Applications Submitted by UNOMEDICAL SDN BHD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K962389 | 06/20/1996 | EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE | UNOMEDICAL SDN BHD |
| K973076 | 08/18/1997 | EUROMEDICAL HAEMATURIA FOLEY CATHETER | UNOMEDICAL SDN BHD |
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