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FDA 510(k)

520 DISPLAY DRIVER- STATUS I

K-Number: K926298 · 1994-05-04

ApplicantVidco, Inc.
Decision Date1994-05-04
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

520 DISPLAY DRIVER- STATUS I is the device name listed in this FDA 510(k) record. The listed applicant is Vidco, Inc.. It received FDA 510(k) clearance on 1994-05-04 under 510(k) number K926298. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 520 DISPLAY DRIVER- STATUS I?

520 DISPLAY DRIVER- STATUS I is a medical device that received FDA 510(k) clearance on 1994-05-04. The listed applicant is Vidco, Inc.. The 510(k) number is K926298.

When did 520 DISPLAY DRIVER- STATUS I receive FDA 510(k) clearance?

520 DISPLAY DRIVER- STATUS I received FDA 510(k) clearance on 1994-05-04, under 510(k) number K926298.

Who is the listed applicant for 520 DISPLAY DRIVER- STATUS I?

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 520 DISPLAY DRIVER- STATUS I?

The FDA product code for 520 DISPLAY DRIVER- STATUS I is DRT.

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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 DRIVERK926219516YT DISPLAY DRIVERK926162580CD DISPLAY DRIVERK890353SMDS460 SURGICAL MONITOR DISPLAY SYSTEM

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Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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