FDA 510(k) Applications Submitted by NEURO SUPPLIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K991769 | 05/24/1999 | CUTANEOUS (BAR) ELECTRODE | NEURO SUPPLIES, INC. |
| K991770 | 05/24/1999 | CUTANEOUS (GROUND) ELECTRODE | NEURO SUPPLIES, INC. |
| K991771 | 05/24/1999 | DIGITAL RING ELECTRDE | NEURO SUPPLIES, INC. |
| K991772 | 05/24/1999 | CUTANEOUS (DISC) ELECTRODE | NEURO SUPPLIES, INC. |
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