Thermoclick
K222057 is the FDA 510(k) clearance record for THERMOCLICK, a class II device, cleared for T&R BIOFAB CO., 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 2 510(k) clearances for T&R BIOFAB CO., Ltd., from to . As of , FDA records show no recalls naming K222057.
Clearance record
- Decision date
- Received
- (511 days to decision)
- Product code
- FLL Continuous Measurement Thermometer
- Regulation
- 21 CFR 880.2910
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- T&R BIOFAB CO., Ltd. 542, Korea Polytechnic University, 237, Sangidaehak-Ro, Siheung-Si, KR
- 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 |
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What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
