| K-number | K901526 |
| Device name | PRO TREATMENT TABLE |
| Applicant | R&R Ent., Inc. |
| Product code | JFB |
| Device class | Class II |
| Decision date | Apr 20, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 890.5880 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov