FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

AllTest Multi-Drug Urine Test Panel; AllTest Multi-Drug Rapid Urine Test Panel

K Number: K242540 · Decision Sep 27, 2024
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
29
Applicant Total
14
Review Days
32

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Basic Information

Device Name
AllTest Multi-Drug Urine Test Panel; AllTest Multi-Drug Rapid Urine Test Panel
K Number
K242540
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hangzhou AllTest Biotech Co., Ltd.
Date Received
August 26, 2024
Decision Date
September 27, 2024
Product Code
NFT
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NFT Test, Amphetamine, Over The Counter

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NFT), ordered by most recent decision date.

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Other Clearances by Hangzhou AllTest Biotech Co., Ltd.

K Number Device Name
K260342 AllTest Strep A Rapid Test
K252607 AllTest Urinary Tract Infection Test
K251053 Shinetell PlusTM Digital Early Pregnancy Test
K242576 AllTest Viral Transport Medium
K250727 AllTest Multi-Drug Rapid Urine Test Cup; AllTest Multi-Drug Urine Test Cup
K244043 AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup
K241978 Shinetell Digital Pregnancy Test
K241428 AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup
K233019 AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest Multi-Drug Rapid Test Cup Rx; AllTest Multi-Drug Rapid Test Panel Rx
K233417 AllTest Fentanyl Urine Test Cassette
Search all 14 clearances from Hangzhou AllTest Biotech Co., Ltd. →