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FDA 510(k)

CT/MRI TOPOGRAPHIC MARKER

K-Number: K930752 · 1993-11-19

ApplicantI.Z.I. Corp.
Decision Date1993-11-19
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT/MRI TOPOGRAPHIC MARKER is the device name listed in this FDA 510(k) record. The listed applicant is I.Z.I. Corp.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K930752. The device is classified under product code JAC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CT/MRI TOPOGRAPHIC MARKER?

CT/MRI TOPOGRAPHIC MARKER is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is I.Z.I. Corp.. The 510(k) number is K930752.

When did CT/MRI TOPOGRAPHIC MARKER receive FDA 510(k) clearance?

CT/MRI TOPOGRAPHIC MARKER received FDA 510(k) clearance on 1993-11-19, under 510(k) number K930752.

Who is the listed applicant for CT/MRI TOPOGRAPHIC MARKER?

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

What is the FDA product code for CT/MRI TOPOGRAPHIC MARKER?

The FDA product code for CT/MRI TOPOGRAPHIC MARKER is JAC.

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Other records listing I.Z.I. 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.

K022074SPHERZK014022MRI LINE MARKERK003736MRI LINE MARKERK994117MR ENHANCERK993742SUPER TISSUEK922287E.Z. PORT(TM) RADIATION THERAPY SKIN MARKERS

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Related Devices (Code: JAC)

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.

K942883DIGITAL I.D. CAMERAMiles Inc., Agfa DivisionK932357FUJI EC ID CAMERAFujifilm Medical System U.S.A., Inc.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak CompanyK923533ADMARKPlanmeca USA, Inc.K925332BENNETT X-RAY ID PLUSBennett X-Ray Technologies

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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