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FDA 510(k)

DUPONT ACA LIQUID BILIRUBIN CALIBRATOR

K-Number: K842222 · 1984-06-05

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1984-06-05
Product Code
DecisionUnknown

Device Summary

DUPONT ACA LIQUID BILIRUBIN CALIBRATOR 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 1984-06-05 under 510(k) number K842222. FDA Decision: Unknown.

Frequently Asked Questions

What is the DUPONT ACA LIQUID BILIRUBIN CALIBRATOR?

DUPONT ACA LIQUID BILIRUBIN CALIBRATOR is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K842222.

When did DUPONT ACA LIQUID BILIRUBIN CALIBRATOR receive FDA 510(k) clearance?

DUPONT ACA LIQUID BILIRUBIN CALIBRATOR received FDA 510(k) clearance on 1984-06-05, under 510(k) number K842222.

Who is the listed applicant for DUPONT ACA LIQUID BILIRUBIN CALIBRATOR?

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.

Related Clinical Trials

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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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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