K202031Substantially Equivalent
Talent-Pro Electromagnetic Stimulator
Remed Co., Ltd., Daejeon, KR / Traditional, Substantially Equivalent
K202031 is the FDA 510(k) clearance record for Talent-Pro Electromagnetic Stimulator, a class II device, cleared for Remed Co., Ltd. on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 3 510(k) clearances for Remed Co., Ltd., from to . As of , FDA records show no recalls naming K202031.
Clearance record
- Decision date
- Received
- (288 days to decision)
- Product code
- IPF Stimulator, Muscle, Powered
- Regulation
- 21 CFR 890.5850
- Device class
- Class II
- Review panel
- Physical Medicine
- Applicant
- Remed Co., Ltd. #301-#303 Migun Techno World Ii, 187, Techno 2-Ro, Daejeon, KR
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code IPF
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 2 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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