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FDA 510(k)

A/T X-RAY 70

K-Number: K024285 · 2003-04-16

ApplicantAir Techniques, Inc.
Decision Date2003-04-16
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

A/T X-RAY 70 is the device name listed in this FDA 510(k) record. The listed applicant is Air Techniques, Inc.. It received FDA 510(k) clearance on 2003-04-16 under 510(k) number K024285. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A/T X-RAY 70?

A/T X-RAY 70 is a medical device that received FDA 510(k) clearance on 2003-04-16. The listed applicant is Air Techniques, Inc.. The 510(k) number is K024285.

When did A/T X-RAY 70 receive FDA 510(k) clearance?

A/T X-RAY 70 received FDA 510(k) clearance on 2003-04-16, under 510(k) number K024285.

Who is the listed applicant for A/T X-RAY 70?

The FDA 510(k) record lists Air Techniques, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A/T X-RAY 70?

The FDA product code for A/T X-RAY 70 is EHD.

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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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