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FDA 510(k)

DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR

K-Number: K922699 · 1992-09-23

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1992-09-23
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR 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 1992-09-23 under 510(k) number K922699. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR?

DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K922699.

When did DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR receive FDA 510(k) clearance?

DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR received FDA 510(k) clearance on 1992-09-23, under 510(k) number K922699.

Who is the listed applicant for DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR?

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 ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR?

The FDA product code for DU PONT ACA MASS CREATIVE KINASE MB (MCKMB) CALIBR is JIS.

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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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