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FDA 510(k)

SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD

K-Number: K885042 · 1988-12-22

Decision Date1988-12-22
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD is the device name listed in this FDA 510(k) record. The listed applicant is Sony Medical Electronics Co.. It received FDA 510(k) clearance on 1988-12-22 under 510(k) number K885042. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD?

SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is Sony Medical Electronics Co.. The 510(k) number is K885042.

When did SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD receive FDA 510(k) clearance?

SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD received FDA 510(k) clearance on 1988-12-22, under 510(k) number K885042.

Who is the listed applicant for SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD?

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

What is the FDA product code for SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD?

The FDA product code for SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD is KQM.

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 Medical Electronics Co. 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 8 devices →

Related Devices (Code: KQM)

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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