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FDA 510(k)

IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE

K-Number: K963628 · 1996-11-07

Decision Date1996-11-07
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Dejarnette Research Systems. It received FDA 510(k) clearance on 1996-11-07 under 510(k) number K963628. 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 IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE?

IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE is a medical device that received FDA 510(k) clearance on 1996-11-07. The listed applicant is Dejarnette Research Systems. The 510(k) number is K963628.

When did IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE receive FDA 510(k) clearance?

IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE received FDA 510(k) clearance on 1996-11-07, under 510(k) number K963628.

Who is the listed applicant for IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE?

The FDA 510(k) record lists Dejarnette Research Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE?

The FDA product code for IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE 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.

Other records listing Dejarnette Research Systems 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.

View all 9 devices →

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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