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FDA 510(k)

TIBC PRETREATMENT KIT

K-Number: K842019 · 1984-06-22

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1984-06-22
Product CodeJQE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TIBC PRETREATMENT KIT 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 1984-06-22 under 510(k) number K842019. The device is classified under product code JQE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIBC PRETREATMENT KIT?

TIBC PRETREATMENT KIT is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K842019.

When did TIBC PRETREATMENT KIT receive FDA 510(k) clearance?

TIBC PRETREATMENT KIT received FDA 510(k) clearance on 1984-06-22, under 510(k) number K842019.

Who is the listed applicant for TIBC PRETREATMENT KIT?

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 TIBC PRETREATMENT KIT?

The FDA product code for TIBC PRETREATMENT KIT is JQE.

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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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