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FDA 510(k)

CHOLESTEROL 1, 2, 3

K-Number: K014018 · 2002-06-24

ApplicantImi
Decision Date2002-06-24
Product CodeLBS
Advisory CommitteeCH
DecisionUnknown

Device Summary

CHOLESTEROL 1, 2, 3 is the device name listed in this FDA 510(k) record. The listed applicant is Imi. It received FDA 510(k) clearance on 2002-06-24 under 510(k) number K014018. The device is classified under product code LBS. It was reviewed by the CH advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CHOLESTEROL 1, 2, 3?

CHOLESTEROL 1, 2, 3 is a medical device that received FDA 510(k) clearance on 2002-06-24. The listed applicant is Imi. The 510(k) number is K014018.

When did CHOLESTEROL 1, 2, 3 receive FDA 510(k) clearance?

CHOLESTEROL 1, 2, 3 received FDA 510(k) clearance on 2002-06-24, under 510(k) number K014018.

Who is the listed applicant for CHOLESTEROL 1, 2, 3?

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

What is the FDA product code for CHOLESTEROL 1, 2, 3?

The FDA product code for CHOLESTEROL 1, 2, 3 is LBS.

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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.

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