FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
cryo-GO Vitrification Device
K Number: K241341
·
Decision Sep 26, 2024
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
49
Applicant Total
4
Review Days
136
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Basic Information
- Device Name
- cryo-GO Vitrification Device
- K Number
- K241341
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.6160
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Fujifilm Irvine Scientific
- Date Received
- May 13, 2024
- Decision Date
- September 26, 2024
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| MQK | Labware, Assisted Reproduction | FDA class 2 | Obstetrics/Gynecology |
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