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FDA 510(k)

SONY LMD-2451MT LCD MONITOR

K-Number: K113203 · 2012-02-24

Decision Date2012-02-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SONY LMD-2451MT LCD MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Sony Electronics, Inc.. It received FDA 510(k) clearance on 2012-02-24 under 510(k) number K113203. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY LMD-2451MT LCD MONITOR?

SONY LMD-2451MT LCD MONITOR is a medical device that received FDA 510(k) clearance on 2012-02-24. The listed applicant is Sony Electronics, Inc.. The 510(k) number is K113203.

When did SONY LMD-2451MT LCD MONITOR receive FDA 510(k) clearance?

SONY LMD-2451MT LCD MONITOR received FDA 510(k) clearance on 2012-02-24, under 510(k) number K113203.

Who is the listed applicant for SONY LMD-2451MT LCD MONITOR?

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

What is the FDA product code for SONY LMD-2451MT LCD MONITOR?

The FDA product code for SONY LMD-2451MT LCD MONITOR is GCJ.

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 Sony Electronics, 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: GCJ)

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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