510(k) K210548
K210548 is an FDA 510(k) premarket notification submitted by Centurion Medical Products for the device "Medline Integrated Arterial Catheter". The FDA issued a decision of Substantially Equivalent on May 17, 2022. The device falls under product code DQX (Wire, Guide, Catheter), a Class II device regulated under 21 CFR 870.1330.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 17, 2022
- Date Received
- Feb 25, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wire, Guide, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1330
- Review Panel
- CV
- Submission Type
- 510(k)