510(k) K260091
K260091 is an FDA 510(k) premarket notification submitted by Inquis Medical for the device "Aventus Introducer Sheath". The FDA issued a decision of Substantially Equivalent on April 13, 2026. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Inquis Medical has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 13, 2026
- Date Received
- January 12, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Introducer, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1340
- Review Panel
- CV
- Submission Type