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FDA 510(k) Applications Submitted by Hangzhou AllTest Biotech Co., Ltd
FDA 510(k) Number
Submission Date
Device Name
Applicant
K182738
09/28/2018
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
Hangzhou AllTest Biotech Co., Ltd
K203272
11/06/2020
Alltest Pregnancy Rapid Combo Test Cassette
Hangzhou AllTest Biotech Co., Ltd
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