FDA 510(k) Applications Submitted by SHANDONG QIAOPAI GROUP CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K073705 | 12/31/2007 | MODEL TW SB, SCALP VEIN SET; MODEL TW LB, STERILE HYPODERMIC NEEDLE | SHANDONG QIAOPAI GROUP CO., LTD |
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