The following data is part of a premarket notification filed by Weyerhaeuser Co. with the FDA for Dripride Disposable Underpad.
| Device ID | K881859 |
| 510k Number | K881859 |
| Device Name: | DRIPRIDE DISPOSABLE UNDERPAD |
| Classification | Bedding, Disposable, Medical |
| 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 | KME |
| CFR Regulation Number | 880.6060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-03 |
| Decision Date | 1988-06-03 |