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FDA 510(k)

CHOLESTEROL RAPID LIQUID REAGENT

K-Number: K972853 · 1997-09-24

ApplicantReagents Applications, Inc.
Decision Date1997-09-24
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHOLESTEROL RAPID LIQUID REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Reagents Applications, Inc.. It received FDA 510(k) clearance on 1997-09-24 under 510(k) number K972853. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOLESTEROL RAPID LIQUID REAGENT?

CHOLESTEROL RAPID LIQUID REAGENT is a medical device that received FDA 510(k) clearance on 1997-09-24. The listed applicant is Reagents Applications, Inc.. The 510(k) number is K972853.

When did CHOLESTEROL RAPID LIQUID REAGENT receive FDA 510(k) clearance?

CHOLESTEROL RAPID LIQUID REAGENT received FDA 510(k) clearance on 1997-09-24, under 510(k) number K972853.

Who is the listed applicant for CHOLESTEROL RAPID LIQUID REAGENT?

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

What is the FDA product code for CHOLESTEROL RAPID LIQUID REAGENT?

The FDA product code for CHOLESTEROL RAPID LIQUID REAGENT is CHH.

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Related Devices (Code: CHH)

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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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