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FDA 510(k)

DUPONT PREP TYPE CS EXTRACTION CARTRIDE

K-Number: K830694 · 1983-04-08

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1983-04-08
Product Code
DecisionSubstantially Equivalent

Device Summary

DUPONT PREP TYPE CS EXTRACTION CARTRIDE 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 1983-04-08 under 510(k) number K830694. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT PREP TYPE CS EXTRACTION CARTRIDE?

DUPONT PREP TYPE CS EXTRACTION CARTRIDE is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K830694.

When did DUPONT PREP TYPE CS EXTRACTION CARTRIDE receive FDA 510(k) clearance?

DUPONT PREP TYPE CS EXTRACTION CARTRIDE received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830694.

Who is the listed applicant for DUPONT PREP TYPE CS EXTRACTION CARTRIDE?

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.

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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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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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