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FDA 510(k)

DU PONT COMPACT DAYLIGHT SYSTEM 2000

K-Number: K922483 · 1992-09-11

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

Device Summary

DU PONT COMPACT DAYLIGHT SYSTEM 2000 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 1992-09-11 under 510(k) number K922483. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT COMPACT DAYLIGHT SYSTEM 2000?

DU PONT COMPACT DAYLIGHT SYSTEM 2000 is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K922483.

When did DU PONT COMPACT DAYLIGHT SYSTEM 2000 receive FDA 510(k) clearance?

DU PONT COMPACT DAYLIGHT SYSTEM 2000 received FDA 510(k) clearance on 1992-09-11, under 510(k) number K922483.

Who is the listed applicant for DU PONT COMPACT DAYLIGHT SYSTEM 2000?

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 2000?

The FDA product code for DU PONT COMPACT DAYLIGHT SYSTEM 2000 is KPX.

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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.

K951851ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAYK953724CRONEX RADIATION THERAPY CASSETTEK953725CRONEX RADIATION THERAPY VERIFICATION CASSETTEK951441DUPONT ACA DIGOXIN (DGN A) METHODK950137URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGEK950136URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE

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Related Devices (Code: KPX)

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.

K945635TRANS X-1000Canon USA, Inc.K935157ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBESRegulatory Consultants TO the Medical Device IndusK934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSVictoreen, Inc.K933035BCM-600TXB C Medical , Ltd.K925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGERAcoma Medical Imaging, Inc.K924423MWX-7440 HIGH SPEED BUCKYMidwest X-Ray Equipment Co.

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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