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FDA 510(k)

ANYRAY PORTABLE X-RAY SYSTEM

K-Number: K081899 · 2008-08-21

ApplicantE-Woo Technology Co., Ltd.
Decision Date2008-08-21
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANYRAY PORTABLE X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is E-Woo Technology Co., Ltd.. It received FDA 510(k) clearance on 2008-08-21 under 510(k) number K081899. 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 ANYRAY PORTABLE X-RAY SYSTEM?

ANYRAY PORTABLE X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-08-21. The listed applicant is E-Woo Technology Co., Ltd.. The 510(k) number is K081899.

When did ANYRAY PORTABLE X-RAY SYSTEM receive FDA 510(k) clearance?

ANYRAY PORTABLE X-RAY SYSTEM received FDA 510(k) clearance on 2008-08-21, under 510(k) number K081899.

Who is the listed applicant for ANYRAY PORTABLE X-RAY SYSTEM?

The FDA 510(k) record lists E-Woo Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANYRAY PORTABLE X-RAY SYSTEM?

The FDA product code for ANYRAY PORTABLE X-RAY SYSTEM is EHD.

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Related Devices (Code: EHD)

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.

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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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