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FDA 510(k)

SPECTRUM 150 DT

K-Number: K851644 · 1985-05-21

ApplicantRaytheon Medical Systems
Decision Date1985-05-21
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPECTRUM 150 DT is the device name listed in this FDA 510(k) record. The listed applicant is Raytheon Medical Systems. It received FDA 510(k) clearance on 1985-05-21 under 510(k) number K851644. 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 SPECTRUM 150 DT?

SPECTRUM 150 DT is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Raytheon Medical Systems. The 510(k) number is K851644.

When did SPECTRUM 150 DT receive FDA 510(k) clearance?

SPECTRUM 150 DT received FDA 510(k) clearance on 1985-05-21, under 510(k) number K851644.

Who is the listed applicant for SPECTRUM 150 DT?

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

What is the FDA product code for SPECTRUM 150 DT?

The FDA product code for SPECTRUM 150 DT 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 Raytheon Medical Systems 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.

K853395RMS-1000 A.K.A. RAYTHEON MEDICAL SYSTEMS-1000

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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