FDA 510(k) Applications Submitted by SEIRIN-AMERICA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K962809 | 07/18/1996 | SEIRIN ACUPUNCTURE NEEDLES | SEIRIN-AMERICA, INC. |
| K963769 | 09/19/1996 | SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES | SEIRIN-AMERICA, INC. |
| K970254 | 01/22/1997 | SEIRIN PYONEX ACUPUNCTURE NEEDLES | SEIRIN-AMERICA, INC. |
| K970260 | 01/23/1997 | SEIRIN JR ACUPUNCTURE NEEDLES | SEIRIN-AMERICA, INC. |
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