FDA 510(k) Applications Submitted by PINNACLE CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072223 | 08/10/2007 | VINYL EXAMINATION GLOVE, POWDERED | PINNACLE CO., LTD. |
| K072227 | 08/10/2007 | VINYL EXAMINATION GLOVE POWDER FREE | PINNACLE CO., LTD. |
| K072228 | 08/10/2007 | SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE) | PINNACLE CO., LTD. |
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