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FDA 510(k)

TRU-VIEW MULTI-CHANNEL DISPLAY

K-Number: K912008 · 1991-10-09

ApplicantGeneral Devices
Decision Date1991-10-09
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRU-VIEW MULTI-CHANNEL DISPLAY is the device name listed in this FDA 510(k) record. The listed applicant is General Devices. It received FDA 510(k) clearance on 1991-10-09 under 510(k) number K912008. 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 TRU-VIEW MULTI-CHANNEL DISPLAY?

TRU-VIEW MULTI-CHANNEL DISPLAY is a medical device that received FDA 510(k) clearance on 1991-10-09. The listed applicant is General Devices. The 510(k) number is K912008.

When did TRU-VIEW MULTI-CHANNEL DISPLAY receive FDA 510(k) clearance?

TRU-VIEW MULTI-CHANNEL DISPLAY received FDA 510(k) clearance on 1991-10-09, under 510(k) number K912008.

Who is the listed applicant for TRU-VIEW MULTI-CHANNEL DISPLAY?

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

What is the FDA product code for TRU-VIEW MULTI-CHANNEL DISPLAY?

The FDA product code for TRU-VIEW MULTI-CHANNEL DISPLAY is DRT.

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Other records listing General Devices as applicant

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Related Devices (Code: DRT)

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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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