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FDA 510(k)

LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR

K-Number: K033899 · 2004-05-20

ApplicantLifestream Technologies, Inc.
Decision Date2004-05-20
Product CodeNFX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Lifestream Technologies, Inc.. It received FDA 510(k) clearance on 2004-05-20 under 510(k) number K033899. The device is classified under product code NFX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR?

LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR is a medical device that received FDA 510(k) clearance on 2004-05-20. The listed applicant is Lifestream Technologies, Inc.. The 510(k) number is K033899.

When did LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR receive FDA 510(k) clearance?

LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR received FDA 510(k) clearance on 2004-05-20, under 510(k) number K033899.

Who is the listed applicant for LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR?

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

What is the FDA product code for LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR?

The FDA product code for LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR is NFX.

Related Clinical Trials

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Other records listing Lifestream Technologies, Inc. as applicant

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.

K000610RESOLUTION CHOLESTEROL MONITORK993096PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR

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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