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FDA 510(k)

ACA THYROXINE CALIBRATOR

K-Number: K833700 · 1983-12-27

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1983-12-27
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA THYROXINE 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 1983-12-27 under 510(k) number K833700. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA THYROXINE CALIBRATOR?

ACA THYROXINE CALIBRATOR is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K833700.

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

ACA THYROXINE CALIBRATOR received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833700.

Who is the listed applicant for ACA THYROXINE 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.

What is the FDA product code for ACA THYROXINE CALIBRATOR?

The FDA product code for ACA THYROXINE CALIBRATOR is JIT.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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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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