Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17
K-Number: K221616 · 2022-08-01
Device Summary
Frequently Asked Questions
What is the Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17?
Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 is a medical device that received FDA 510(k) clearance on 2022-08-01. It is manufactured by Caf Medical Solutions, Inc.. The 510(k) number is K221616.
When was Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 approved by the FDA?
Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 received FDA 510(k) clearance on 2022-08-01, under approval number K221616.
What company makes Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17?
Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 is manufactured by Caf Medical Solutions, Inc..
What is the FDA product code for Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17?
The FDA product code for Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 is MHX.
Related Clinical Trials
Related PubMed Literature
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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.