510(k) K173481
K173481 is an FDA 510(k) premarket notification submitted by STERIS Corporation for the device "Amsco Evolution Medium Steam Sterilizer". The FDA issued a decision of Substantially Equivalent on Mar 9, 2018. The device falls under product code FLE (Sterilizer, Steam), a Class II device regulated under 21 CFR 880.6880. STERIS Corporation has 204 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 9, 2018
- Date Received
- Nov 13, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sterilizer, Steam
- Device Class
- Class II
- Regulation Number
- 880.6880
- Review Panel
- HO
- Submission Type
- 510(k)