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FDA 510(k)

QUALITROL CRP CONTROL SET

K-Number: K961829 · 1996-08-19

ApplicantConsolidated Technologies, Inc.
Decision Date1996-08-19
Product CodeDCK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUALITROL CRP CONTROL SET 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 1996-08-19 under 510(k) number K961829. The device is classified under product code DCK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUALITROL CRP CONTROL SET?

QUALITROL CRP CONTROL SET is a medical device that received FDA 510(k) clearance on 1996-08-19. The listed applicant is Consolidated Technologies, Inc.. The 510(k) number is K961829.

When did QUALITROL CRP CONTROL SET receive FDA 510(k) clearance?

QUALITROL CRP CONTROL SET received FDA 510(k) clearance on 1996-08-19, under 510(k) number K961829.

Who is the listed applicant for QUALITROL CRP CONTROL SET?

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 QUALITROL CRP CONTROL SET?

The FDA product code for QUALITROL CRP CONTROL SET is DCK.

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Related Devices (Code: DCK)

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.

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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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