FDA 510(k) Applications Submitted by QINGDAO SHUANG DIE LATEX PRODUCTION CO.,LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K012653 | 08/13/2001 | MALE LATEX CONDOM | QINGDAO SHUANG DIE LATEX PRODUCTION CO.,LTD |
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