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FDA 510(k)

A-TAP (previously called Arthrotap)

K-Number: K231900 · 2023-07-25

Decision Date2023-07-25
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A-TAP (previously called Arthrotap) is the device name listed in this FDA 510(k) record. The listed applicant is Elcam Medical Acal. It received FDA 510(k) clearance on 2023-07-25 under 510(k) 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. The listed applicant is Elcam Medical Acal. The 510(k) number is K231900.

When did A-TAP (previously called Arthrotap) receive FDA 510(k) clearance?

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

Who is the listed applicant for A-TAP (previously called Arthrotap)?

The FDA 510(k) record lists Elcam Medical Acal as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Elcam Medical Acal as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.