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FDA 510(k)

PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF

K-Number: K032628 · 2004-02-02

Decision Date2004-02-02
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF is the device name listed in this FDA 510(k) record. The listed applicant is United Radiology Systems, Inc.. It received FDA 510(k) clearance on 2004-02-02 under 510(k) number K032628. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF?

PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF is a medical device that received FDA 510(k) clearance on 2004-02-02. The listed applicant is United Radiology Systems, Inc.. The 510(k) number is K032628.

When did PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF receive FDA 510(k) clearance?

PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF received FDA 510(k) clearance on 2004-02-02, under 510(k) number K032628.

Who is the listed applicant for PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF?

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

What is the FDA product code for PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF?

The FDA product code for PORTABLE X-RAY UNIT, MODELS PXP-15/20/40HF is IZL.

Related Clinical Trials

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.

Other records listing United Radiology Systems, Inc. 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: IZL)

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.

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