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

Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set

K Number: K180073 · Decision Aug 29, 2018
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
258
Applicant Total
1
Review Days
232

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Basic Information

Device Name
Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set
K Number
K180073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6180
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Vitavitro Bio-Tech Co., Ltd.
Date Received
January 9, 2018
Decision Date
August 29, 2018
Product Code
MQL
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
MQL Media, Reproductive

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