FDA 510(k)

DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR

K-Number: K914917 · 1991-12-13

ApplicantE.I. Dupont DE Nemours & Co., Inc.

Decision Date1991-12-13

Product CodeJIX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DU PONT TOTAL PROTEIN/ALBUMIN 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 1991-12-13 under 510(k) number K914917. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR?

DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR is a medical device that received FDA 510(k) clearance on 1991-12-13. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K914917.

When did DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR receive FDA 510(k) clearance?

DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR received FDA 510(k) clearance on 1991-12-13, under 510(k) number K914917.

Who is the listed applicant for DU PONT TOTAL PROTEIN/ALBUMIN 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 DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR?

The FDA product code for DU PONT TOTAL PROTEIN/ALBUMIN CALIBRATOR is JIX.

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Related Devices (Code: JIX)

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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.