Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SONY PVM-2551MD OLED MONITOR

K-Number: K120611 · 2012-06-28

Decision Date2012-06-28
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SONY PVM-2551MD OLED 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 2012-06-28 under 510(k) number K120611. 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 PVM-2551MD OLED MONITOR?

SONY PVM-2551MD OLED MONITOR is a medical device that received FDA 510(k) clearance on 2012-06-28. The listed applicant is Sony Electronics, Inc.. The 510(k) number is K120611.

When did SONY PVM-2551MD OLED MONITOR receive FDA 510(k) clearance?

SONY PVM-2551MD OLED MONITOR received FDA 510(k) clearance on 2012-06-28, under 510(k) number K120611.

Who is the listed applicant for SONY PVM-2551MD OLED 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 PVM-2551MD OLED MONITOR?

The FDA product code for SONY PVM-2551MD OLED 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑