MY01, Inc.
MY01, Inc. holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2026, with 1 FDA device recall on record.
Top product codes for MY01, Inc.
FDA recalls by MY01, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by MY01, Inc.
- K251900 — MY01 Continuous Compartmental Pressure Monitor
- K242997 — MY01 Continuous Compartmental Pressure Monitor
- K220952 — MY01 Continuous Compartmental Pressure Monitor
- K210525 — MY01 Continuous Compartmental Pressure Monitor
- K202635 — MY01 Continuous Compartmental Pressure Monitor
- K193321 — MY01 Continuous Compartmental Pressure Monitor
Data sourced from openFDA. This site is unofficial and independent of the FDA.