510(k) K171520
K171520 is an FDA 510(k) premarket notification submitted by Sterizign Precision Technologies, LLC for the device "SteriZign Signatur Device Protection System". The FDA issued a decision of Substantially Equivalent on Feb 7, 2018. The device falls under product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories), a Class II device regulated under 21 CFR 880.6850.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 7, 2018
- Date Received
- May 24, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- Device Class
- Class II
- Regulation Number
- 880.6850
- Review Panel
- HO
- Submission Type
- 510(k)