510(k) K200017
K200017 is an FDA 510(k) premarket notification submitted by Eclipse Medcorp, LLC for the device "Eclipse DermaFlex Cannula". The FDA issued a decision of Substantially Equivalent on Nov 5, 2020. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. Eclipse Medcorp, LLC has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 5, 2020
- Date Received
- Jan 3, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Needle, Hypodermic, Single Lumen
- Device Class
- Class II
- Regulation Number
- 880.5570
- Review Panel
- HO
- Submission Type
- 510(k)