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FDA 510(k)

J&S HDL CHOLESTEROL PRECIPITATING REAGENT

K-Number: K900218 · 1990-06-18

ApplicantJ.S. Medical Assoc.
Decision Date1990-06-18
Product CodeLBL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

J&S HDL CHOLESTEROL PRECIPITATING REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is J.S. Medical Assoc.. It received FDA 510(k) clearance on 1990-06-18 under 510(k) number K900218. The device is classified under product code LBL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J&S HDL CHOLESTEROL PRECIPITATING REAGENT?

J&S HDL CHOLESTEROL PRECIPITATING REAGENT is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K900218.

When did J&S HDL CHOLESTEROL PRECIPITATING REAGENT receive FDA 510(k) clearance?

J&S HDL CHOLESTEROL PRECIPITATING REAGENT received FDA 510(k) clearance on 1990-06-18, under 510(k) number K900218.

Who is the listed applicant for J&S HDL CHOLESTEROL PRECIPITATING REAGENT?

The FDA 510(k) record lists J.S. Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for J&S HDL CHOLESTEROL PRECIPITATING REAGENT?

The FDA product code for J&S HDL CHOLESTEROL PRECIPITATING REAGENT is LBL.

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Other records listing J.S. Medical Assoc. 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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