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FDA 510(k)

Medwell Technology Ltd Syringes, various sizes

K-Number: K212764 · 2022-11-04

ApplicantMedwell Technology, Ltd.
Decision Date2022-11-04
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Medwell Technology Ltd Syringes, various sizes is a medical device manufactured by Medwell Technology, Ltd.. It received FDA 510(k) clearance on 2022-11-04 under approval number K212764. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medwell Technology Ltd Syringes, various sizes?

Medwell Technology Ltd Syringes, various sizes is a medical device that received FDA 510(k) clearance on 2022-11-04. It is manufactured by Medwell Technology, Ltd.. The 510(k) number is K212764.

When was Medwell Technology Ltd Syringes, various sizes approved by the FDA?

Medwell Technology Ltd Syringes, various sizes received FDA 510(k) clearance on 2022-11-04, under approval number K212764.

What company makes Medwell Technology Ltd Syringes, various sizes?

Medwell Technology Ltd Syringes, various sizes is manufactured by Medwell Technology, Ltd..

What is the FDA product code for Medwell Technology Ltd Syringes, various sizes?

The FDA product code for Medwell Technology Ltd Syringes, various sizes is FMF.

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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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