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FDA 510(k)

LIPOPROTEIN PROFILING SYSTEM

K-Number: K770948 · 1977-07-15

Decision Date1977-07-15
Product CodeJHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIPOPROTEIN PROFILING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1977-07-15 under 510(k) number K770948. The device is classified under product code JHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPOPROTEIN PROFILING SYSTEM?

LIPOPROTEIN PROFILING SYSTEM is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K770948.

When did LIPOPROTEIN PROFILING SYSTEM receive FDA 510(k) clearance?

LIPOPROTEIN PROFILING SYSTEM received FDA 510(k) clearance on 1977-07-15, under 510(k) number K770948.

Who is the listed applicant for LIPOPROTEIN PROFILING SYSTEM?

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

What is the FDA product code for LIPOPROTEIN PROFILING SYSTEM?

The FDA product code for LIPOPROTEIN PROFILING SYSTEM is JHL.

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 Beckman Instruments, 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.

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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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