510(k) K240002
K240002 is an FDA 510(k) premarket notification submitted by Gimbo Medical Technology Shenzhen Co., Ltd. for the device "G-Vitri Vitrification Straw". The FDA issued a decision of Substantially Equivalent on June 14, 2024. The device falls under product code MQK (Labware, Assisted Reproduction), a Class II device regulated under 21 CFR 884.6160. Gimbo Medical Technology Shenzhen Co., Ltd. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 14, 2024
- Date Received
- January 2, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Labware, Assisted Reproduction
- Device Class
- Class II
- Regulation Number
- 884.6160
- Review Panel
- OB
- Submission Type