510(k) K220952
K220952 is an FDA 510(k) premarket notification submitted by MY01, Inc. for the device "MY01 Continuous Compartmental Pressure Monitor". The FDA issued a decision of Substantially Equivalent on May 24, 2022. The device falls under product code LXC (Monitor, Pressure, Intracompartmental), a Class U device. MY01, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 24, 2022
- Date Received
- April 1, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Monitor, Pressure, Intracompartmental
- Device Class
- Class U
- Regulation Number
- Review Panel
- OR
- Submission Type