K781106Substantially Equivalent
Thermometer, Exacta Temp
S.M.B. Celsius Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
K781106 is the FDA 510(k) clearance record for THERMOMETER, EXACTA TEMP, a class II device, cleared for S.M.B. Celsius Co., Inc. on under FDA product code FLK (Thermometer, Clinical Mercury). FDA records list one 510(k) clearance for S.M.B. Celsius Co., Inc. As of , FDA records show no recalls naming K781106.
Clearance record
- Decision date
- Received
- (38 days to decision)
- Product code
- FLK Thermometer, Clinical Mercury
- Regulation
- 21 CFR 880.2920
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- S.M.B. Celsius Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code FLK
Trailing 12 monthsFDA records hold no clearances under product code FLK 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.
