FDA 510(k) Applications Submitted by SPECIALIZED HEALTH PRODUCTS INTERNATIONAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070449 | 02/15/2007 | LUMILOC (TM) SAFETY INTRODUCER NEEDLE | SPECIALIZED HEALTH PRODUCTS INTERNATIONAL, INC. |
| K073050 | 10/29/2007 | SAFESTEP MAX POWER-INJECTABLE INFUSION SET | SPECIALIZED HEALTH PRODUCTS INTERNATIONAL, INC. |
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