Probe Cover: JZ-KBT-001, JZ-KBT-002, JZ-KBT-005, JZ-KBT-007, JZ-KBT-008, JZ-KBT-009, JZ-KBT-010, JZ-KBT-015, JZ-KBT-025, JZ-KBT-026
K202009 is the FDA 510(k) clearance record for Probe Cover: JZ-KBT-001, JZ-KBT-002, JZ-KBT-005, JZ-KBT-007, JZ-KBT-008, JZ-KBT-009, JZ-KBT-010, JZ-KBT-015, JZ-KBT-025, JZ-KBT-026, a class II device, cleared for Shenzhen Juzhong Technology 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 one 510(k) clearance for Shenzhen Juzhong Technology Co., Ltd. As of , FDA records show no recalls naming K202009.
Clearance record
- Decision date
- Received
- (244 days to decision)
- Product code
- FLL Continuous Measurement Thermometer
- Regulation
- 21 CFR 880.2910
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- Shenzhen Juzhong Technology Co., Ltd. Block B, Floor 3, Bldg. 38, Sanhe Village,, Shenzhen, 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 |
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