510(k) K130179
K130179 is an FDA 510(k) premarket notification submitted by Medimop Medical Projects, Ltd. for the device "MP VIAL ADAPTER 13MM". The FDA issued a decision of Substantially Equivalent on August 8, 2013. The device falls under product code LHI (Set, I.V. Fluid Transfer), a Class II device regulated under 21 CFR 880.5440. Medimop Medical Projects, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 8, 2013
- Date Received
- January 25, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, I.V. Fluid Transfer
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type