510(k) K132293
K132293 is an FDA 510(k) premarket notification submitted by Marine Polymer Technologies for the device "SYVEK RADIAL BAND". The FDA issued a decision of Substantially Equivalent on July 31, 2014. The device falls under product code DXC (Clamp, Vascular), a Class II device regulated under 21 CFR 870.4450. Marine Polymer Technologies has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 31, 2014
- Date Received
- July 23, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clamp, Vascular
- Device Class
- Class II
- Regulation Number
- 870.4450
- Review Panel
- CV
- Submission Type