510(k) K073705 ยท FMI Needle, Hypodermic, Single Lumen
MODEL TW SB, SCALP VEIN SET; MODEL TW LB, STERILE HYPODERMIC NEEDLE
| Applicant | Shandong Qiaopai Group Co., Ltd., Zibo, CN |
| Decision | Substantially Equivalent, Mar 24, 2008 |
| Received | Dec 31, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073705
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.