Product code FNP
- Device name
- Urinal
- Medical specialty
- General Hospital
- Device class
- 1
- Regulation number
- 880.6730
- Review panel
- HO
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- Y
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K771738 | MALE URINAL | Bemis Health Care | 1977-09-28 |
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