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FDA 510(k)

DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM

K-Number: K893775 · 1989-07-25

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1989-07-25
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM 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 1989-07-25 under 510(k) number K893775. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM?

DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K893775.

When did DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM receive FDA 510(k) clearance?

DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM received FDA 510(k) clearance on 1989-07-25, under 510(k) number K893775.

Who is the listed applicant for DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM?

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 DIMENSION PSID CLINICAL CHEMISTRY SYSTEM?

The FDA product code for DU PONT DIMENSION PSID CLINICAL CHEMISTRY SYSTEM is JQW.

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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: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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