FDA 510(k)

ACQA

K-Number: K113086 · 2012-01-13

ApplicantTexas Medical Imaging Consultants

Decision Date2012-01-13

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ACQA is the device name listed in this FDA 510(k) record. The listed applicant is Texas Medical Imaging Consultants. It received FDA 510(k) clearance on 2012-01-13 under 510(k) number K113086. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACQA?

ACQA is a medical device that received FDA 510(k) clearance on 2012-01-13. The listed applicant is Texas Medical Imaging Consultants. The 510(k) number is K113086.

When did ACQA receive FDA 510(k) clearance?

ACQA received FDA 510(k) clearance on 2012-01-13, under 510(k) number K113086.

Who is the listed applicant for ACQA?

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

What is the FDA product code for ACQA?

The FDA product code for ACQA is KPS.

Related Devices (Code: KPS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.