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FDA 510(k)

516YT DISPLAY DRIVER

K-Number: K926219 · 1993-12-16

ApplicantVidco, Inc.
Decision Date1993-12-16
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

516YT DISPLAY DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Vidco, Inc.. It received FDA 510(k) clearance on 1993-12-16 under 510(k) number K926219. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 516YT DISPLAY DRIVER?

516YT DISPLAY DRIVER is a medical device that received FDA 510(k) clearance on 1993-12-16. The listed applicant is Vidco, Inc.. The 510(k) number is K926219.

When did 516YT DISPLAY DRIVER receive FDA 510(k) clearance?

516YT DISPLAY DRIVER received FDA 510(k) clearance on 1993-12-16, under 510(k) number K926219.

Who is the listed applicant for 516YT DISPLAY DRIVER?

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

What is the FDA product code for 516YT DISPLAY DRIVER?

The FDA product code for 516YT DISPLAY DRIVER is DXJ.

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.

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Other records listing Vidco, 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.

K972880MDP2000 MEDICAL DATA PROCESSORK934093580CDR DISPLAY DRIVERK932894620CSR DISPLAY DRIVERK926298520 DISPLAY DRIVER- STATUS IK926162580CD DISPLAY DRIVERK890353SMDS460 SURGICAL MONITOR DISPLAY SYSTEM

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Related Devices (Code: DXJ)

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.

K212003ESSENZ Patient MonitorLivanova Deutschland, GmbHK212208Philips IntelliVue GuardianSoftware (Rev. E.0X)Philips Medizin Systeme Boeblingen GmbHK201162Essence 55SP Large Monitor SystemShenyang Torch-Bigtide Digital Technology Co., Ltd.K173107Vios Central Station Monitor Software, Vios Central Server SoftwareVios Medical, Inc.K180534Philips IntelliVue GuardianSoftwarePhilips Medizin Systeme Boeblingen GmbHK173381Nexxis ORBarco N.V.

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.

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