The following data is part of a premarket notification filed by Weyerhaeuser Co. with the FDA for Dripride Ultra Incontinent Pad.
| Device ID | K883895 |
| 510k Number | K883895 |
| Device Name: | DRIPRIDE ULTRA INCONTINENT PAD |
| Classification | Garment, Protective, For Incontinence |
| Applicant | WEYERHAEUSER CO. 2101 L STREET, N.W. Washington, DC 20037 |
| Contact | Howard M Holstein |
| Correspondent | Howard M Holstein WEYERHAEUSER CO. 2101 L STREET, N.W. Washington, DC 20037 |
| Product Code | EYQ |
| CFR Regulation Number | 876.5920 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-14 |
| Decision Date | 1989-01-30 |