K792642Substantially Equivalent
The Variable Load Kenetic Energizer
W.F. Pogue, Mchenry IL / Traditional, Substantially Equivalent
K792642 is the FDA 510(k) clearance record for THE VARIABLE LOAD KENETIC ENERGIZER, a class I device, cleared for W.F. Pogue on under FDA product code ION (Exerciser, Non-Measuring). FDA records list one 510(k) clearance for W.F. Pogue. As of , FDA records show no recalls naming K792642.
Clearance record
- Decision date
- Received
- (33 days to decision)
- Product code
- ION Exerciser, Non-Measuring
- Regulation
- 21 CFR 890.5370
- Device class
- Class I
- Review panel
- Physical Medicine
- Applicant
- W.F. Pogue 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code ION
Trailing 12 monthsFDA records hold no clearances under product code ION 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 |
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.
