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FDA 510(k)

SMDS460 SURGICAL MONITOR DISPLAY SYSTEM

K-Number: K890353 · 1989-03-02

ApplicantVidco, Inc.
Decision Date1989-03-02
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SMDS460 SURGICAL MONITOR DISPLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vidco, Inc.. It received FDA 510(k) clearance on 1989-03-02 under 510(k) number K890353. 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 SMDS460 SURGICAL MONITOR DISPLAY SYSTEM?

SMDS460 SURGICAL MONITOR DISPLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-03-02. The listed applicant is Vidco, Inc.. The 510(k) number is K890353.

When did SMDS460 SURGICAL MONITOR DISPLAY SYSTEM receive FDA 510(k) clearance?

SMDS460 SURGICAL MONITOR DISPLAY SYSTEM received FDA 510(k) clearance on 1989-03-02, under 510(k) number K890353.

Who is the listed applicant for SMDS460 SURGICAL MONITOR DISPLAY SYSTEM?

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 SMDS460 SURGICAL MONITOR DISPLAY SYSTEM?

The FDA product code for SMDS460 SURGICAL MONITOR DISPLAY SYSTEM is DXJ.

Related Clinical Trials

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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 IK926219516YT DISPLAY DRIVERK926162580CD DISPLAY DRIVER

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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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