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FDA 510(k)

MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B

K-Number: K881898 · 1988-06-14

Decision Date1988-06-14
Product CodeMSJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B is the device name listed in this FDA 510(k) record. The listed applicant is Atlantic Antibodies. It received FDA 510(k) clearance on 1988-06-14 under 510(k) number K881898. 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 MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B?

MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B is a medical device that received FDA 510(k) clearance on 1988-06-14. The listed applicant is Atlantic Antibodies. The 510(k) number is K881898.

When did MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B receive FDA 510(k) clearance?

MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B received FDA 510(k) clearance on 1988-06-14, under 510(k) number K881898.

Who is the listed applicant for MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B?

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

What is the FDA product code for MODIFIED SPQ(TM) TEST SYSTEM FOR APOLIPOPROTEIN B?

The FDA product code for MODIFIED SPQ(TM) TEST SYSTEM FOR 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 Atlantic Antibodies 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 18 devices →

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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