Hightop® Home Use Fentanyl/Norfentanyl Urine Rapid Test Panel; Hightop® Fentanyl/Norfentanyl Urine Rapid Test Panel
FDA 510(k) clearance K241969 · decided 2024-08-14
Clearance details
- K-number
- K241969
- Device name
- Hightop® Home Use Fentanyl/Norfentanyl Urine Rapid Test Panel; Hightop® Fentanyl/Norfentanyl Urine Rapid Test Panel
- Applicant
- Qingdao Hightop Biotech Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2024-07-05
- Decision date
- 2024-08-14
- Days to decision
- 40 days
- Clearance type
- Traditional
- Product code
- NGL
- Device class
- 2
- Regulation number
- 862.3650
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Qingdao, CN
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.