510(k) K153025
K153025 is an FDA 510(k) premarket notification submitted by Turbett Surgical, LLC for the device "Turbett Surgical Container". The FDA issued a decision of Substantially Equivalent on January 14, 2016. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. Turbett Surgical, LLC has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 2016
- Date Received
- October 16, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wrap, Sterilization
- Device Class
- Class II
- Regulation Number
- 880.6850
- Review Panel
- HO
- Submission Type