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FDA 510(k)

MF SAFECATH

K-Number: K192230 · 2020-04-23

ApplicantMedifirst Co., Ltd.
Decision Date2020-04-23
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MF SAFECATH is a medical device manufactured by Medifirst Co., Ltd.. It received FDA 510(k) clearance on 2020-04-23 under approval number K192230. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MF SAFECATH?

MF SAFECATH is a medical device that received FDA 510(k) clearance on 2020-04-23. It is manufactured by Medifirst Co., Ltd.. The 510(k) number is K192230.

When was MF SAFECATH approved by the FDA?

MF SAFECATH received FDA 510(k) clearance on 2020-04-23, under approval number K192230.

What company makes MF SAFECATH?

MF SAFECATH is manufactured by Medifirst Co., Ltd..

What is the FDA product code for MF SAFECATH?

The FDA product code for MF SAFECATH is FOZ.

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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.

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