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FDA 510(k)

SERIES OF DIAGNOSTIC PHANTOMS

K-Number: K834465 · 1984-02-21

ApplicantCirs, Inc.
Decision Date1984-02-21
Product CodeIXG
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SERIES OF DIAGNOSTIC PHANTOMS is the device name listed in this FDA 510(k) record. The listed applicant is Cirs, Inc.. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K834465. The device is classified under product code IXG. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES OF DIAGNOSTIC PHANTOMS?

SERIES OF DIAGNOSTIC PHANTOMS is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Cirs, Inc.. The 510(k) number is K834465.

When did SERIES OF DIAGNOSTIC PHANTOMS receive FDA 510(k) clearance?

SERIES OF DIAGNOSTIC PHANTOMS received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834465.

Who is the listed applicant for SERIES OF DIAGNOSTIC PHANTOMS?

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

What is the FDA product code for SERIES OF DIAGNOSTIC PHANTOMS?

The FDA product code for SERIES OF DIAGNOSTIC PHANTOMS is IXG.

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Related Devices (Code: IXG)

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.

K913243BENNETT X-RAY HORIZ RADIO FLOAT/HI-LO ELEV TABLEBennett X-Ray Corp.K852528BONE DENSITY CT PHANTOMComputerized Imaging Reference Systems, Inc.K840131COMPUTED TOMOGRAPHY CALIBRATION PHANTImatron, Inc.

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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