510(k) K202593
K202593 is an FDA 510(k) premarket notification submitted by Turbett Surgical, Inc. for the device "Turbett Instrument Pod". The FDA issued a decision of Substantially Equivalent on May 19, 2021. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. Turbett Surgical, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 19, 2021
- Date Received
- September 8, 2020
- 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