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FDA 510(k)

HEART CHECK APOLIPOPROTEIN-B

K-Number: K881433 · 1988-04-21

Decision Date1988-04-21
Product CodeMSJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HEART CHECK APOLIPOPROTEIN-B is the device name listed in this FDA 510(k) record. The listed applicant is Northwest Biotech. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881433. The device is classified under product code MSJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEART CHECK APOLIPOPROTEIN-B?

HEART CHECK APOLIPOPROTEIN-B is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Northwest Biotech. The 510(k) number is K881433.

When did HEART CHECK APOLIPOPROTEIN-B receive FDA 510(k) clearance?

HEART CHECK APOLIPOPROTEIN-B received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881433.

Who is the listed applicant for HEART CHECK APOLIPOPROTEIN-B?

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

What is the FDA product code for HEART CHECK APOLIPOPROTEIN-B?

The FDA product code for HEART CHECK APOLIPOPROTEIN-B is MSJ.

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 Northwest Biotech 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: MSJ)

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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