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FDA 510(k)

A-TAP (previously called Arthrotap)

K-Number: K231900 · 2023-07-25

ApplicantElcam Medical Acal
Decision Date2023-07-25
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A-TAP (previously called Arthrotap) is a medical device manufactured by Elcam Medical Acal. It received FDA 510(k) clearance on 2023-07-25 under approval number K231900. 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 A-TAP (previously called Arthrotap)?

A-TAP (previously called Arthrotap) is a medical device that received FDA 510(k) clearance on 2023-07-25. It is manufactured by Elcam Medical Acal. The 510(k) number is K231900.

When was A-TAP (previously called Arthrotap) approved by the FDA?

A-TAP (previously called Arthrotap) received FDA 510(k) clearance on 2023-07-25, under approval number K231900.

What company makes A-TAP (previously called Arthrotap)?

A-TAP (previously called Arthrotap) is manufactured by Elcam Medical Acal.

What is the FDA product code for A-TAP (previously called Arthrotap)?

The FDA product code for A-TAP (previously called Arthrotap) 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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