FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Cryotop®US-flash and Cryotop®US-scoop

K Number: K181469 · Decision Nov 9, 2018
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
49
Applicant Total
13
Review Days
158

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Basic Information

Device Name
Cryotop®US-flash and Cryotop®US-scoop
K Number
K181469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kitazato Corporation
Date Received
June 4, 2018
Decision Date
November 9, 2018
Product Code
MQK
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
MQK Labware, Assisted Reproduction

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