The following data is part of a premarket notification filed by Smartmissimo Technologies Pte Ltd with the FDA for Powerdot Pd-01mt.
Device ID | K181759 |
510k Number | K181759 |
Device Name: | PowerDot PD-01MT |
Classification | Stimulator, Muscle, Powered |
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 | IPF |
Subsequent Product Code | GZJ |
Subsequent Product Code | NGX |
Subsequent Product Code | NUH |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-07-02 |
Decision Date | 2018-11-09 |