The following data is part of a premarket notification filed by Rich-mar Corp. with the FDA for The Probe 100.
| Device ID | K844466 |
| 510k Number | K844466 |
| Device Name: | THE PROBE 100 |
| Classification | Stimulator, Muscle, Powered |
| Applicant | RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 |
| Contact | Richards |
| Correspondent | Richards RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-11-19 |
| Decision Date | 1985-02-21 |