K032652Substantially Equivalent
Rs-4I Muscle Stimulator Family
RS Medical, Vancouver WA / Traditional, Substantially Equivalent
K032652 is the FDA 510(k) clearance record for RS-4I MUSCLE STIMULATOR FAMILY, a class II device, cleared for Rs Medical on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 10 510(k) clearances for Rs Medical, from to . As of , FDA records show one recall naming K032652.
Clearance record
- Decision date
- Received
- (15 days to decision)
- Product code
- IPF Stimulator, Muscle, Powered
- Regulation
- 21 CFR 890.5850
- Device class
- Class II
- Review panel
- Physical Medicine
- Applicant
- Rs Medical 14401 SE First St., Vancouver WA
- 510(k) summary
- Summary PDF
- Third party review
- Yes
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 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
