510(k) K142116
K142116 is an FDA 510(k) premarket notification submitted by Spectranetics, Inc. for the device "LLD EZ". The FDA issued a decision of Substantially Equivalent on August 12, 2014. The device falls under product code DRB (Stylet, Catheter), a Class II device regulated under 21 CFR 870.1380. Spectranetics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 12, 2014
- Date Received
- August 4, 2014
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stylet, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1380
- Review Panel
- CV
- Submission Type