FDA 510(k)

JPI X-RAY GRID

K-Number: K945327 · 1995-01-20

Decision Date1995-01-20

Product CodeIXJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

JPI X-RAY GRID is the device name listed in this FDA 510(k) record. The listed applicant is Jpi America, Inc.. It received FDA 510(k) clearance on 1995-01-20 under 510(k) number K945327. 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 JPI X-RAY GRID?

JPI X-RAY GRID is a medical device that received FDA 510(k) clearance on 1995-01-20. The listed applicant is Jpi America, Inc.. The 510(k) number is K945327.

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

JPI X-RAY GRID received FDA 510(k) clearance on 1995-01-20, under 510(k) number K945327.

Who is the listed applicant for JPI X-RAY GRID?

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

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

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

Other records listing Jpi America, Inc. 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.

K052341AJEX 9015/135H PORTABLE X-RAY K945328JPI X-RAY FILM CASSETTE

Related Devices (Code: IXJ)

K964025MITAYA ALUMINUM INTERSPACED X-RAY GRIDX-Ray Accessory Corp.K963893FIBRE INTERSPACED X-RAY GRIDSmit Rontgen K962338RADIOGRAPHIC GRIDUnidex Group, Inc.K954294HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZESThermotrex Corp.K945697SK S-RAY GRIDSSeibu Techno Coproration 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.