510(k) K152826
K152826 is an FDA 510(k) premarket notification submitted by Centrix, Inc. for the device "NoCord". The FDA issued a decision of Substantially Equivalent on May 27, 2016. The device falls under product code ELW (Material, Impression), a Class II device regulated under 21 CFR 872.3660. Centrix, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 27, 2016
- Date Received
- September 29, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Material, Impression
- Device Class
- Class II
- Regulation Number
- 872.3660
- Review Panel
- DE
- Submission Type