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FDA 510(k)

SONY VIDEO PRINTERS, UP SERIES

K-Number: K882958 · 1988-08-04

Decision Date1988-08-04
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SONY VIDEO PRINTERS, UP SERIES 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 1988-08-04 under 510(k) number K882958. 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 VIDEO PRINTERS, UP SERIES?

SONY VIDEO PRINTERS, UP SERIES is a medical device that received FDA 510(k) clearance on 1988-08-04. The listed applicant is Sony Medical Electronics Co.. The 510(k) number is K882958.

When did SONY VIDEO PRINTERS, UP SERIES receive FDA 510(k) clearance?

SONY VIDEO PRINTERS, UP SERIES received FDA 510(k) clearance on 1988-08-04, under 510(k) number K882958.

Who is the listed applicant for SONY VIDEO PRINTERS, UP SERIES?

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 VIDEO PRINTERS, UP SERIES?

The FDA product code for SONY VIDEO PRINTERS, UP SERIES 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.

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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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