The following data is part of a premarket notification filed by Dymedso Inc. with the FDA for Frequencer Model V2x.
| Device ID | K100749 |
| 510k Number | K100749 |
| Device Name: | FREQUENCER MODEL V2X |
| Classification | Percussor, Powered-electric |
| Applicant | DYMEDSO INC. 127 MAIN ST. Springfield, VT 05156 -0826 |
| Contact | Jean Bigoney |
| Correspondent | Jean Bigoney DYMEDSO INC. 127 MAIN ST. Springfield, VT 05156 -0826 |
| Product Code | BYI |
| CFR Regulation Number | 868.5665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-03-16 |
| Decision Date | 2010-08-31 |
| Summary: | summary |