510(k) K231484
K231484 is an FDA 510(k) premarket notification submitted by Pureway Compliance, Inc. for the device "PureWay 1.4 Quart Sharps Collector". The FDA issued a decision of Substantially Equivalent on September 14, 2023. The device falls under product code MMK (Container, Sharps), a Class II device regulated under 21 CFR 880.5570. Pureway Compliance, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 14, 2023
- Date Received
- May 23, 2023
- 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