The following data is part of a premarket notification filed by Dermanetics Corp. with the FDA for System 2500 Medical Waterbed.
| Device ID | K894723 |
| 510k Number | K894723 |
| Device Name: | SYSTEM 2500 MEDICAL WATERBED |
| Classification | Bed, Flotation Therapy, Powered |
| Applicant | DERMANETICS CORP. 741 W. 17TH ST. Long Beach, CA 90813 |
| Contact | Scott Postle |
| Correspondent | Scott Postle DERMANETICS CORP. 741 W. 17TH ST. Long Beach, CA 90813 |
| Product Code | IOQ |
| CFR Regulation Number | 890.5170 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-07-25 |
| Decision Date | 1989-08-17 |