The following data is part of a premarket notification filed by Medical Management Service, Inc. with the FDA for Weyland Extension Vibrator.
| Device ID | K822413 |
| 510k Number | K822413 |
| Device Name: | WEYLAND EXTENSION VIBRATOR |
| Classification | Table, Physical Therapy, Multi Function |
| Applicant | MEDICAL MANAGEMENT SERVICE, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JFB |
| CFR Regulation Number | 890.5880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-08-10 |
| Decision Date | 1983-06-08 |