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FDA 510(k)

DU PONT LINX HD-25 LASR IMAGER

K-Number: K923042 · 1992-11-09

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1992-11-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DU PONT LINX HD-25 LASR IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K923042. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT LINX HD-25 LASR IMAGER?

DU PONT LINX HD-25 LASR IMAGER is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K923042.

When did DU PONT LINX HD-25 LASR IMAGER receive FDA 510(k) clearance?

DU PONT LINX HD-25 LASR IMAGER received FDA 510(k) clearance on 1992-11-09, under 510(k) number K923042.

Who is the listed applicant for DU PONT LINX HD-25 LASR IMAGER?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DU PONT LINX HD-25 LASR IMAGER?

The FDA product code for DU PONT LINX HD-25 LASR IMAGER is LLZ.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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Related Devices (Code: LLZ)

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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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