K842276Substantially Equivalent
Sunmaster
Mt. Hood Mfr., Inc., Mchenry IL / Traditional, Substantially Equivalent
K842276 is the FDA 510(k) clearance record for SUNMASTER, a class II device, cleared for Mt. Hood Mfr., Inc. on under FDA product code IOB (Lamp, Infrared, Non Heating). FDA records list one 510(k) clearance for Mt. Hood Mfr., Inc. As of , FDA records show no recalls naming K842276.
Clearance record
- Decision date
- Received
- (38 days to decision)
- Product code
- IOB Lamp, Infrared, Non Heating
- Regulation
- 21 CFR 890.5500
- Device class
- Class II
- Review panel
- Physical Medicine
- Applicant
- Mt. Hood Mfr., Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code IOB
Trailing 12 monthsFDA records hold no clearances under product code IOB 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.
