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FDA 510(k)

GRIDGIL

K-Number: K941626 · 1994-05-13

ApplicantGilardoni S.P.A.
Decision Date1994-05-13
Product CodeIXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GRIDGIL is the device name listed in this FDA 510(k) record. The listed applicant is Gilardoni S.P.A.. It received FDA 510(k) clearance on 1994-05-13 under 510(k) number K941626. 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 GRIDGIL?

GRIDGIL is a medical device that received FDA 510(k) clearance on 1994-05-13. The listed applicant is Gilardoni S.P.A.. The 510(k) number is K941626.

When did GRIDGIL receive FDA 510(k) clearance?

GRIDGIL received FDA 510(k) clearance on 1994-05-13, under 510(k) number K941626.

Who is the listed applicant for GRIDGIL?

The FDA 510(k) record lists Gilardoni S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRIDGIL?

The FDA product code for GRIDGIL 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.K963893FIBRE INTERSPACED X-RAY GRIDSmit RontgenK962338RADIOGRAPHIC 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.

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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