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FDA 510(k)

PC TELERADIOLOGY(TM)

K-Number: K925050 · 1993-05-03

Decision Date1993-05-03
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PC TELERADIOLOGY(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Arizona State Radiology. It received FDA 510(k) clearance on 1993-05-03 under 510(k) number K925050. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PC TELERADIOLOGY(TM)?

PC TELERADIOLOGY(TM) is a medical device that received FDA 510(k) clearance on 1993-05-03. The listed applicant is Arizona State Radiology. The 510(k) number is K925050.

When did PC TELERADIOLOGY(TM) receive FDA 510(k) clearance?

PC TELERADIOLOGY(TM) received FDA 510(k) clearance on 1993-05-03, under 510(k) number K925050.

Who is the listed applicant for PC TELERADIOLOGY(TM)?

The FDA 510(k) record lists Arizona State Radiology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PC TELERADIOLOGY(TM)?

The FDA product code for PC TELERADIOLOGY(TM) is LMD.

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.

Related Devices (Code: LMD)

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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