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FDA 510(k)

CATHODE RAY TUBE MED. DISPLAY

K-Number: K781256 · 1978-09-20

ApplicantRae Medical Corp.
Decision Date1978-09-20
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHODE RAY TUBE MED. DISPLAY is the device name listed in this FDA 510(k) record. The listed applicant is Rae Medical Corp.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781256. 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 CATHODE RAY TUBE MED. DISPLAY?

CATHODE RAY TUBE MED. DISPLAY is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Rae Medical Corp.. The 510(k) number is K781256.

When did CATHODE RAY TUBE MED. DISPLAY receive FDA 510(k) clearance?

CATHODE RAY TUBE MED. DISPLAY received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781256.

Who is the listed applicant for CATHODE RAY TUBE MED. DISPLAY?

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

What is the FDA product code for CATHODE RAY TUBE MED. DISPLAY?

The FDA product code for CATHODE RAY TUBE MED. DISPLAY 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 Rae Medical Corp. 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.

K830321VENTURE II MONITORING SYSTEMK781255DIGITAL PANEL METER

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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