The following data is part of a premarket notification filed by Smartmissimo Technologies Pte Ltd with the FDA for Powerdot(r) Pd-01 Muscle Stimulator (with Powerdot(r) Mobile Application).
| Device ID | K150078 |
| 510k Number | K150078 |
| Device Name: | PowerDot(R) PD-01 Muscle Stimulator (with PowerDot(R) Mobile Application) |
| Classification | Stimulator, Muscle, Powered, For Muscle Conditioning |
| Applicant | Smartmissimo Technologies Pte Ltd #28-01, SGX Centre II, 4 Shenton Way Singapore, SG 068807 |
| Contact | Alexey Pisarev |
| Correspondent | Alexey Pisarev Smartmissimo Technologies Pte Ltd #28-01, SGX Centre II, 4 Shenton Way Singapore, SG 068807 |
| Product Code | NGX |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-01-15 |
| Decision Date | 2015-09-30 |
| Summary: | summary |