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FDA 510(k)

ACA THYROXINE UPTAKE CALIBRATOR

K-Number: K833702 · 1984-01-04

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1984-01-04
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA THYROXINE UPTAKE 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 1984-01-04 under 510(k) number K833702. 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 UPTAKE CALIBRATOR?

ACA THYROXINE UPTAKE CALIBRATOR is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K833702.

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

ACA THYROXINE UPTAKE CALIBRATOR received FDA 510(k) clearance on 1984-01-04, under 510(k) number K833702.

Who is the listed applicant for ACA THYROXINE UPTAKE 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 UPTAKE CALIBRATOR?

The FDA product code for ACA THYROXINE UPTAKE CALIBRATOR is JIT.

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

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Related Devices (Code: JIT)

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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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