MY01 Continuous Compartmental Pressure Monitor
K-Number: K220952 · 2022-05-24
Device Summary
Frequently Asked Questions
What is the MY01 Continuous Compartmental Pressure Monitor?
MY01 Continuous Compartmental Pressure Monitor is a medical device that received FDA 510(k) clearance on 2022-05-24. The listed applicant is MY01, Inc.. The 510(k) number is K220952.
When did MY01 Continuous Compartmental Pressure Monitor receive FDA 510(k) clearance?
MY01 Continuous Compartmental Pressure Monitor received FDA 510(k) clearance on 2022-05-24, under 510(k) number K220952.
Who is the listed applicant for MY01 Continuous Compartmental Pressure Monitor?
The FDA 510(k) record lists MY01, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MY01 Continuous Compartmental Pressure Monitor?
The FDA product code for MY01 Continuous Compartmental Pressure Monitor is LXC.
Other records listing MY01, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LXC)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.