FDA 510(k)

CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL

K-Number: K905457 · 1991-04-16

ApplicantConsolidated Technologies, Inc.

Decision Date1991-04-16

Product CodeDIF

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Technologies, Inc.. It received FDA 510(k) clearance on 1991-04-16 under 510(k) number K905457. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL?

CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Consolidated Technologies, Inc.. The 510(k) number is K905457.

When did CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL receive FDA 510(k) clearance?

CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL received FDA 510(k) clearance on 1991-04-16, under 510(k) number K905457.

Who is the listed applicant for CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL?

The FDA 510(k) record lists Consolidated Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL?

The FDA product code for CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL is DIF.

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Other records listing Consolidated Technologies, Inc. as applicant

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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.