FDA 510(k) Applications Submitted by HAKKO SHOJI CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020307 | 01/29/2002 | LAP DISC 120 X 120MM X 2CM #LD111; LAP DISC 120 X 120MM X 7CM #LD112 | HAKKO SHOJI CO., LTD. |
| K961151 | 03/22/1996 | SPINAL NEEDLES | HAKKO SHOJI CO., LTD. |
| K961152 | 03/22/1996 | TUOHY EPIDURAL NEEDLES | HAKKO SHOJI CO., LTD. |
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