510(k) clearance
Liquick X-treme, Liquick X-treme Plus
- 510(k) number
- K261418
- Applicant
- Teleflex Medical
- Decision date
- Sep 23, 2026
- Date received
- Apr 30, 2026
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Product code
- EZD
- Device type
- Catheter, Straight
- Device class
- Class II
- Regulation
- 21 CFR 876.5130
- Advisory committee
- Gastroenterology, Urology
- Statement or summary
- Summary
- Third party
- N
- Location
- Athlone, IE