510(k) K222232
K222232 is an FDA 510(k) premarket notification submitted by Bard Access Systems, Inc. for the device "Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly". The FDA issued a decision of Substantially Equivalent on August 24, 2022. The device falls under product code LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days), a Class II device regulated under 21 CFR 880.5970. Bard Access Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 2022
- Date Received
- July 25, 2022
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- Device Class
- Class II
- Regulation Number
- 880.5970
- Review Panel
- HO
- Submission Type