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FDA 510(k)

DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI

K-Number: K901017 · 1990-05-15

Decision Date1990-05-15
Product CodeJFJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI 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 1990-05-15 under 510(k) number K901017. The device is classified under product code JFJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI?

DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K901017.

When did DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI receive FDA 510(k) clearance?

DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI received FDA 510(k) clearance on 1990-05-15, under 510(k) number K901017.

Who is the listed applicant for DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI?

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 ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI?

The FDA product code for DU PONT ANALYST ANALYTICAL TEST ROTOR:CHEM-14,CALI is JFJ.

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.

View all 253 devices →

Related Devices (Code: JFJ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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