Winstim
K102190 is the FDA 510(k) clearance record for WINSTIM, a class II device, cleared for Johari Digital Healthcare , Ltd. on under FDA product code IMG (Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat). FDA records list 10 510(k) clearances for Johari Digital Healthcare , Ltd., from to . As of , FDA records show no recalls naming K102190.
Clearance record
- Decision date
- Received
- (226 days to decision)
- Product code
- IMG Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
- Regulation
- 21 CFR 890.5860
- Device class
- Class II
- Review panel
- Physical Medicine
- Applicant
- Johari Digital Healthcare , Ltd. G-582,583, E.p.i.p., Jodhpur ,Rajasthan, IN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code IMG
Trailing 12 monthsFDA records hold no clearances under product code IMG in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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