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FDA 510(k)

ACA ACETAMINOPHEN CALIBRATOR

K-Number: K842549 · 1984-08-16

Decision Date1984-08-16
Product Code
DecisionSubstantially Equivalent

Device Summary

ACA ACETAMINOPHEN 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 1984-08-16 under 510(k) number K842549. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA ACETAMINOPHEN CALIBRATOR?

ACA ACETAMINOPHEN CALIBRATOR is a medical device that received FDA 510(k) clearance on 1984-08-16. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K842549.

When did ACA ACETAMINOPHEN CALIBRATOR receive FDA 510(k) clearance?

ACA ACETAMINOPHEN CALIBRATOR received FDA 510(k) clearance on 1984-08-16, under 510(k) number K842549.

Who is the listed applicant for ACA ACETAMINOPHEN 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.

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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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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