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FDA 510(k)

ULTRA HDL

K-Number: K051962 · 2005-08-25

Decision Date2005-08-25
Product CodeLBS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTRA HDL is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2005-08-25 under 510(k) number K051962. The device is classified under product code LBS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA HDL?

ULTRA HDL is a medical device that received FDA 510(k) clearance on 2005-08-25. The listed applicant is Abbott Laboratories. The 510(k) number is K051962.

When did ULTRA HDL receive FDA 510(k) clearance?

ULTRA HDL received FDA 510(k) clearance on 2005-08-25, under 510(k) number K051962.

Who is the listed applicant for ULTRA HDL?

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

What is the FDA product code for ULTRA HDL?

The FDA product code for ULTRA HDL is LBS.

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 Abbott Laboratories 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.

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Related Devices (Code: LBS)

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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