POWDERED LATEX PATIENT EXAMINATION GLOVES — Shinemound Enterprise, Inc. (510(k) K051913)
POWDERED LATEX PATIENT EXAMINATION GLOVES — Shinemound Enterprise, Inc. (510(k) K051913) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: POWDERED LATEX PATIENT EXAMINATION GLOVES; Applicant: Shinemound Enterprise, Inc.; Clearance track: 510(k).
| Device name | POWDERED LATEX PATIENT EXAMINATION GLOVES |
|---|---|
| Applicant | Shinemound Enterprise, Inc. |
| Clearance track | 510(k) |
| Submission number | K051913 |
| Decision | Substantially Equivalent |
| Decision date | 2005-09-30 |
| Date received | 2005-07-15 |
| Product code | LYY |
| Device class | 1 |
| Medical specialty | General Hospital |
| Applicant location | MA, US |
| Source | openFDA device |
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