FDA 510(k)

X-MARX

K-Number: K911873 · 1991-07-19

Decision Date1991-07-19

Product CodeJAC

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

X-MARX is the device name listed in this FDA 510(k) record. The listed applicant is Macbrud Corp. Medical Div.. It received FDA 510(k) clearance on 1991-07-19 under 510(k) number K911873. 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 X-MARX?

X-MARX is a medical device that received FDA 510(k) clearance on 1991-07-19. The listed applicant is Macbrud Corp. Medical Div.. The 510(k) number is K911873.

When did X-MARX receive FDA 510(k) clearance?

X-MARX received FDA 510(k) clearance on 1991-07-19, under 510(k) number K911873.

Who is the listed applicant for X-MARX?

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

What is the FDA product code for X-MARX?

The FDA product code for X-MARX is JAC.

Other records listing Macbrud Corp. Medical Div. 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.

K913049SLIP-PRUF-CLINGER K900282NEEDLE-SHIELD K891090SPECBOARD

Related Devices (Code: JAC)

K942883DIGITAL I.D. CAMERAMiles Inc., Agfa Division K930752CT/MRI TOPOGRAPHIC MARKERI.Z.I. Corp.K932357FUJI EC ID CAMERAFujifilm Medical System U.S.A., Inc.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak Company K923533ADMARKPlanmeca USA, Inc.

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.