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FDA 510(k) Applications Submitted by Shenzhen VitaVitro Biotech Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K240307
02/02/2024
VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
Shenzhen VitaVitro Biotech Co., Ltd.
K240523
02/23/2024
VitaVitro« Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro« Double Lumen Oocyte Retrieval Needle (ORND-17G)
Shenzhen VitaVitro Biotech Co., Ltd.
K191063
04/22/2019
1-Step Culture Medium
Shenzhen VitaVitro Biotech Co., Ltd.
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