ACA ACETAMINOPHEN CALIBRATOR
K-Number: K842549 · 1984-08-16
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Device Summary
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.
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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