510(k) K242968

Device
Giftlife® Single-Step Medium Plus
Applicant
Gimbo Medical Technology Shenzhen Co., Ltd.
510(k) number
K242968
Product code
MQL
Decision
Substantially Equivalent (SESE)
Decision date
2024-11-22
Date received
2024-09-26
Regulation
884.6180
Classification name
Media, Reproductive
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Leo Guo
Address
601, Bldg. C5, # 459 Qiaokai Rd., Fenghuang St. Guangming District Shenzhen CN 518107 518107

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
06976438300392Single Step Medium PlusGimbo Medical Technology Shenzhen Co., Ltd.2025-01-20
06976438300385Single Step Medium PlusGimbo Medical Technology Shenzhen Co., Ltd.2025-01-20

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