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FDA 510(k)

ECLIPSE ICA CHOLESTEROL

K-Number: K905145 · 1991-02-26

ApplicantBiotope, Inc.
Decision Date1991-02-26
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ECLIPSE ICA CHOLESTEROL is the device name listed in this FDA 510(k) record. The listed applicant is Biotope, Inc.. It received FDA 510(k) clearance on 1991-02-26 under 510(k) number K905145. 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 ECLIPSE ICA CHOLESTEROL?

ECLIPSE ICA CHOLESTEROL is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Biotope, Inc.. The 510(k) number is K905145.

When did ECLIPSE ICA CHOLESTEROL receive FDA 510(k) clearance?

ECLIPSE ICA CHOLESTEROL received FDA 510(k) clearance on 1991-02-26, under 510(k) number K905145.

Who is the listed applicant for ECLIPSE ICA CHOLESTEROL?

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

What is the FDA product code for ECLIPSE ICA CHOLESTEROL?

The FDA product code for ECLIPSE ICA CHOLESTEROL 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 Biotope, 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.

View all 7 devices →

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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