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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