The following data is part of a premarket notification filed by Rich-mar Corp. with the FDA for Rich-mar Spina-mobilizor.
| Device ID | K861832 |
| 510k Number | K861832 |
| Device Name: | RICH-MAR SPINA-MOBILIZOR |
| Classification | Equipment, Traction, Powered |
| Applicant | RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 |
| Product Code | ITH |
| CFR Regulation Number | 890.5900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-05-13 |
| Decision Date | 1986-06-27 |