Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEBO Wound Dressing

K-Number: K222657 · 2022-10-18

Decision Date2022-10-18
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

MEBO Wound Dressing is a medical device manufactured by Mebo Life Science, Inc.. It received FDA 510(k) clearance on 2022-10-18 under approval number K222657. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEBO Wound Dressing?

MEBO Wound Dressing is a medical device that received FDA 510(k) clearance on 2022-10-18. It is manufactured by Mebo Life Science, Inc.. The 510(k) number is K222657.

When was MEBO Wound Dressing approved by the FDA?

MEBO Wound Dressing received FDA 510(k) clearance on 2022-10-18, under approval number K222657.

What company makes MEBO Wound Dressing?

MEBO Wound Dressing is manufactured by Mebo Life Science, Inc..

What is the FDA product code for MEBO Wound Dressing?

The FDA product code for MEBO Wound Dressing is FRO. This falls under the Anesthesiology category.

Related Clinical Trials

Related PubMed Literature

Other Devices by Mebo Life Science, Inc.

Related Devices (Code: FRO)

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.