510(k) K221974
K221974 is an FDA 510(k) premarket notification submitted by Omeq Medical , Ltd. for the device "EpiFinder". The FDA issued a decision of Substantially Equivalent on Apr 16, 2023. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 16, 2023
- Date Received
- Jul 5, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Piston
- Device Class
- Class II
- Regulation Number
- 880.5860
- Review Panel
- HO
- Submission Type
- 510(k)