The following data is part of a premarket notification filed by Verimed Holdings, Inc. with the FDA for Verimed Myo/prems.
| Device ID | K874212 |
| 510k Number | K874212 |
| Device Name: | VERIMED MYO/PREMS |
| Classification | Stimulator, Muscle, Powered |
| Applicant | VERIMED HOLDINGS, INC. 1001 N.W. 62ND STREET, SUITE 212 Fort Lauderdale, FL 33309 |
| Contact | William Mee |
| Correspondent | William Mee VERIMED HOLDINGS, INC. 1001 N.W. 62ND STREET, SUITE 212 Fort Lauderdale, FL 33309 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-16 |
| Decision Date | 1988-08-08 |