510(k) K182071
K182071 is an FDA 510(k) premarket notification submitted by Cook Incorporated for the device "Multi-Sideport Catheter Infusion Set". The FDA issued a decision of Substantially Equivalent on Apr 25, 2019. The device falls under product code KRA (Catheter, Continuous Flush), a Class II device regulated under 21 CFR 870.1210. Cook Incorporated has 174 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 25, 2019
- Date Received
- Aug 1, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Continuous Flush
- Device Class
- Class II
- Regulation Number
- 870.1210
- Review Panel
- CV
- Submission Type
- 510(k)