510(k) K170513
K170513 is an FDA 510(k) premarket notification submitted by Mauzer USA, LLC for the device "MAUSER PG II Sharps Container". The FDA issued a decision of Substantially Equivalent on November 1, 2017. The device falls under product code MMK (Container, Sharps), a Class II device regulated under 21 CFR 880.5570.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 1, 2017
- Date Received
- February 21, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Container, Sharps
- Device Class
- Class II
- Regulation Number
- 880.5570
- Review Panel
- HO
- Submission Type