510(k) K252672

Device
CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)
Applicant
Casebioscience, Inc.
510(k) number
K252672
Product code
MQL
Decision
Substantially Equivalent (SESE)
Decision date
2026-02-20
Date received
2025-08-25
Regulation
884.6180
Classification name
Media, Reproductive
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Monica Mezezi
Address
24 Norwich St. E. Guelph CA N1H2G6 N1H2G6

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code MQL

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K241833V-GRADVitromed GmbH2025-03-21
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K240176V-VITFREEZE and V-VITWARMVitromed GmbH2024-09-13
K233846Vitrification Solution Set and Warming Solution SetEcmpc, LLC2024-08-27