510(k) K173694
K173694 is an FDA 510(k) premarket notification submitted by Tso3, Inc. for the device "STERIZONE VP4 Sterilizer". The FDA issued a decision of Substantially Equivalent on March 13, 2018. The device falls under product code PJJ (Two Or More Sterilant Sterilizer), a Class II device regulated under 21 CFR 880.6860. Tso3, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 13, 2018
- Date Received
- December 1, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Two Or More Sterilant Sterilizer
- Device Class
- Class II
- Regulation Number
- 880.6860
- Review Panel
- HO
- Submission Type
Intended for use in terminal sterilization of cleaned, rinsed, and dried metal and non-metal reusable medical devices in health care facilities.