FREQUENCER
Percussor, Powered-electric
DYMEDSO INC.
The following data is part of a premarket notification filed by Dymedso Inc. with the FDA for Frequencer.
Pre-market Notification Details
| Device ID | K103176 |
| 510k Number | K103176 |
| Device Name: | FREQUENCER |
| Classification | Percussor, Powered-electric |
| Applicant | DYMEDSO INC. 127 MAIN ST. PO BOX 826 Springfield, VT 05156 -0826 |
| Contact | Jean Bigoney |
| Correspondent | Jean Bigoney DYMEDSO INC. 127 MAIN ST. PO BOX 826 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 | 2010-10-28 |
| Decision Date | 2011-01-26 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B402DYMV23 | K103176 | 000 |
| B401DYMV2X0 | K103176 | 000 |
| B401DYMV230 | K103176 | 000 |
Trademark Results [FREQUENCER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FREQUENCER 76517724 3348967 Live/Registered |
DYMEDSO INC. 2003-05-02 |
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