510(k) K232388
K232388 is an FDA 510(k) premarket notification submitted by Ningbo Dizegens Medical Science Co.,Ltd for the device "High Pressure Tubing". The FDA issued a decision of Substantially Equivalent on November 21, 2023. The device falls under product code DXT (Injector And Syringe, Angiographic), a Class II device regulated under 21 CFR 870.1650. Ningbo Dizegens Medical Science Co.,Ltd has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 21, 2023
- Date Received
- August 9, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Injector And Syringe, Angiographic
- Device Class
- Class II
- Regulation Number
- 870.1650
- Review Panel
- HO
- Submission Type