Single and Multi-Drug Rapid Test Panel With Adulteration (Urine), Single and Multi-Drug Rapid Test Panel (Urine), Single and Multi-Drug Rapid Test Cup With Adulteration (Urine), Single and Multi-Drug Rapid Test Cup (Urine), Single Drug Rapid Test Dipstick (Urine), Single and Multi-Drug Home Rapid Test Panel (Urine), Single and Multi-Drug Home Rapid Test Cup (Urine), Single Drug Home Rapid Test Dipstick (Urine)
K182738 is the FDA 510(k) clearance record for Single and Multi-Drug Rapid Test Panel With Adulteration (Urine), Single and Multi-Drug Rapid Test Panel (Urine), Single and Multi-Drug Rapid Test Cup With Adulteration (Urine), Single and Multi-Drug Rapid Test Cup (Urine), Single Drug Rapid Test Dipstick (Urine), Single and Multi-Drug Home Rapid Test Panel (Urine), Single and Multi-Drug Home Rapid Test Cup (Urine), Single Drug Home Rapid Test Dipstick (Urine), a class II device, cleared for Hangzhou AllTest Biotech Co., Ltd. on under FDA product code DKZ (Enzyme Immunoassay, Amphetamine). FDA records list 14 510(k) clearances for Hangzhou AllTest Biotech Co., Ltd., from to . As of , FDA records show no recalls naming K182738.
Clearance record
- Decision date
- Received
- (180 days to decision)
- Product code
- DKZ Enzyme Immunoassay, Amphetamine
- Regulation
- 21 CFR 862.3100
- Device class
- Class II
- Review panel
- Clinical Toxicology
- Applicant
- Hangzhou AllTest Biotech Co., Ltd. #550 Yinhai St., Hangzhou, Hangzhou, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DKZ
Trailing 12 monthsFDA records hold no clearances under product code DKZ 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 |
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