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FDA 510(k)

FIBRE INTERSPACED X-RAY GRID

K-Number: K963893 · 1996-11-07

ApplicantSmit Rontgen
Decision Date1996-11-07
Product CodeIXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FIBRE INTERSPACED X-RAY GRID is the device name listed in this FDA 510(k) record. The listed applicant is Smit Rontgen. It received FDA 510(k) clearance on 1996-11-07 under 510(k) number K963893. The device is classified under product code IXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBRE INTERSPACED X-RAY GRID?

FIBRE INTERSPACED X-RAY GRID is a medical device that received FDA 510(k) clearance on 1996-11-07. The listed applicant is Smit Rontgen. The 510(k) number is K963893.

When did FIBRE INTERSPACED X-RAY GRID receive FDA 510(k) clearance?

FIBRE INTERSPACED X-RAY GRID received FDA 510(k) clearance on 1996-11-07, under 510(k) number K963893.

Who is the listed applicant for FIBRE INTERSPACED X-RAY GRID?

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

What is the FDA product code for FIBRE INTERSPACED X-RAY GRID?

The FDA product code for FIBRE INTERSPACED X-RAY GRID is IXJ.

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Related Devices (Code: IXJ)

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.

K964025MITAYA ALUMINUM INTERSPACED X-RAY GRIDX-Ray Accessory Corp.K962338RADIOGRAPHIC GRIDUnidex Group, Inc.K954294HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZESThermotrex Corp.K945697SK S-RAY GRIDSSeibu Techno CoprorationK945327JPI X-RAY GRIDJpi America, Inc.K941626GRIDGILGilardoni S.P.A.

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.

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