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FDA 510(k)

REAL-TIME SPECTRUM ANALYZER

K-Number: K830628 · 1983-06-02

ApplicantDiagnostic Electronics Corp.
Decision Date1983-06-02
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REAL-TIME SPECTRUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Electronics Corp.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K830628. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAL-TIME SPECTRUM ANALYZER?

REAL-TIME SPECTRUM ANALYZER is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Diagnostic Electronics Corp.. The 510(k) number is K830628.

When did REAL-TIME SPECTRUM ANALYZER receive FDA 510(k) clearance?

REAL-TIME SPECTRUM ANALYZER received FDA 510(k) clearance on 1983-06-02, under 510(k) number K830628.

Who is the listed applicant for REAL-TIME SPECTRUM ANALYZER?

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

What is the FDA product code for REAL-TIME SPECTRUM ANALYZER?

The FDA product code for REAL-TIME SPECTRUM ANALYZER is DXG.

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Other records listing Diagnostic Electronics 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.

K861023DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLERK860651MICRON, MICROVASCULAR DOPPLER

Related Devices (Code: DXG)

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.

K253092Argos Infinity (Rev. 1.0)Retia Medical Systems, Inc.K251275VitalStream ART Connect; VitalStream-HemoCaretaker MedicalK232048Cogent™ Hemodynamic Monitoring System; Cogent™ HMSIcu MedicalK212529Hypotension Decision Assist Model HDA-OR2Directed Systems, Ltd.K192169PulsioFlex Monitoring System with ProAQT SensorPulsion Medical Systems SEK193179EV1000 Clinical PlatformEdwards Lifesciences, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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