Class Class II

AllTest Multi-Drug Urine Test Panel; AllTest Multi-Drug Rapid Urine Test Panel (K242540)

K242540 2024-09-27 Traditional
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Description

AllTest Multi-Drug Urine Test Panel; AllTest Multi-Drug Rapid Urine Test Panel by Hangzhou AllTest Biotech Co., Ltd. — FDA 510(k) cleared clinical toxicology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242540
Clearance Date2024-09-27
Clearance TypeTraditional
Product CodeNFT
Regulation Number862.3100

Categories

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