510(k) K810311
K810311 is an FDA 510(k) premarket notification submitted by The Hilrad Co. for the device "STERI-VERS". The FDA issued a decision of Substantially Equivalent on April 17, 1981. The device falls under product code LDS (Device, Pasteurization, Hot Water), a Class II device regulated under 21 CFR 880.6991.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 17, 1981
- Date Received
- February 5, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Pasteurization, Hot Water
- Device Class
- Class II
- Regulation Number
- 880.6991
- Review Panel
- HO
- Submission Type