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FDA 510(k)

PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR

K-Number: K993096 · 1999-12-20

Decision Date1999-12-20
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM 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 1999-12-20 under 510(k) number K993096. 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 PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR?

PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Lifestream Technologies, Inc.. The 510(k) number is K993096.

When did PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR receive FDA 510(k) clearance?

PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR received FDA 510(k) clearance on 1999-12-20, under 510(k) number K993096.

Who is the listed applicant for PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM 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 PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR?

The FDA product code for PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR is CHH.

Related Clinical Trials

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.

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.

Related Devices (Code: CHH)

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.

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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