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FDA 510(k)

DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II)

K-Number: K924552 · 1992-12-07

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1992-12-07
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II) 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 1992-12-07 under 510(k) number K924552. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II)?

DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II) is a medical device that received FDA 510(k) clearance on 1992-12-07. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K924552.

When did DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II) receive FDA 510(k) clearance?

DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II) received FDA 510(k) clearance on 1992-12-07, under 510(k) number K924552.

Who is the listed applicant for DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II)?

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 COMPACT DAYLIGHT SYSTEM II (CDS II)?

The FDA product code for DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II) is IXW.

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

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Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

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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