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FDA 510(k)

DRYSTAR AXYS, MODEL EYZ4E

K-Number: K072680 · 2007-10-25

ApplicantAgfa Healthcare Corporation
Decision Date2007-10-25
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DRYSTAR AXYS, MODEL EYZ4E is the device name listed in this FDA 510(k) record. The listed applicant is Agfa Healthcare Corporation. It received FDA 510(k) clearance on 2007-10-25 under 510(k) number K072680. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRYSTAR AXYS, MODEL EYZ4E?

DRYSTAR AXYS, MODEL EYZ4E is a medical device that received FDA 510(k) clearance on 2007-10-25. The listed applicant is Agfa Healthcare Corporation. The 510(k) number is K072680.

When did DRYSTAR AXYS, MODEL EYZ4E receive FDA 510(k) clearance?

DRYSTAR AXYS, MODEL EYZ4E received FDA 510(k) clearance on 2007-10-25, under 510(k) number K072680.

Who is the listed applicant for DRYSTAR AXYS, MODEL EYZ4E?

The FDA 510(k) record lists Agfa Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRYSTAR AXYS, MODEL EYZ4E?

The FDA product code for DRYSTAR AXYS, MODEL EYZ4E is LMC.

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Related Devices (Code: LMC)

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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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