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FDA 510(k)

INTERAD 520

K-Number: K833821 · 1984-01-13

ApplicantInterad Systems, Inc.
Decision Date1984-01-13
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERAD 520 is the device name listed in this FDA 510(k) record. The listed applicant is Interad Systems, Inc.. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K833821. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERAD 520?

INTERAD 520 is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Interad Systems, Inc.. The 510(k) number is K833821.

When did INTERAD 520 receive FDA 510(k) clearance?

INTERAD 520 received FDA 510(k) clearance on 1984-01-13, under 510(k) number K833821.

Who is the listed applicant for INTERAD 520?

The FDA 510(k) record lists Interad Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERAD 520?

The FDA product code for INTERAD 520 is IYX.

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 Interad Systems, 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.

K834087MODEL XLEK834307ULTRASOUND SCANNER XLK813162INTERAD WHOLE BODY CT SCANNER

Related Devices (Code: IYX)

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.

K230221QDOSE® Multi-purpose Voxel Dosimetry (Personalized Dosimetry in Molecular Radiotherapy)Versant Medical Physics and Radiation SafetyK2125873D-RD-SRadiopharmaceutical Imaging and Dosimetry, LLCK163687OLINDA EXMHermes Medical Solutions ABK160933Discovery NM 750b BopsyGE HealthcareK162052Sentinella 102, Sentinella 102 HorusGeneral Equipment For Medical Imaging (Oncovision-K123408ERGO IMAGING SYSTEMDigirad Corp.

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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