Infrared Ear Thermometer, Models Tm819, Tm820, Tm817, Tm810a, Tm810b, Tm818 and Tm818a
K102935 is the FDA 510(k) clearance record for INFRARED EAR THERMOMETER, MODELS TM819, TM820, TM817, TM810A, TM810B, TM818 AND TM818A, a class II device, cleared for Kingtech Enterprise, Ltd. on under FDA product code FLL (Continuous Measurement Thermometer). FDA's definition for product code FLL reads: "A continuous measurement thermometer is a clinical electronic thermometer indicated to measure the body or skin temperature of a person continuously or in specified intervals. Under this regulation, this product code represents non-exempt...". FDA records list 3 510(k) clearances for Kingtech Enterprise, Ltd., from to . As of , FDA records show no recalls naming K102935.
Clearance record
- Decision date
- Received
- (235 days to decision)
- Product code
- FLL Continuous Measurement Thermometer
- Regulation
- 21 CFR 880.2910
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- Kingtech Enterprise, Ltd. Farm Village, Da Ling Shan Town, Dongguan, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code FLL
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 1 |
| 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.
