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FDA 510(k)

MEASELISA TEST KIT

K-Number: K821762 · 1982-07-30

ApplicantM.A. Bioproducts
Decision Date1982-07-30
Product CodeLJB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MEASELISA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is M.A. Bioproducts. It received FDA 510(k) clearance on 1982-07-30 under 510(k) number K821762. The device is classified under product code LJB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEASELISA TEST KIT?

MEASELISA TEST KIT is a medical device that received FDA 510(k) clearance on 1982-07-30. The listed applicant is M.A. Bioproducts. The 510(k) number is K821762.

When did MEASELISA TEST KIT receive FDA 510(k) clearance?

MEASELISA TEST KIT received FDA 510(k) clearance on 1982-07-30, under 510(k) number K821762.

Who is the listed applicant for MEASELISA TEST KIT?

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

What is the FDA product code for MEASELISA TEST KIT?

The FDA product code for MEASELISA TEST KIT is LJB.

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Other records listing M.A. Bioproducts 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.

K822883HERPELISA KITK823804MYCOPLASMELISA TEST KITK830045MUMPSELISA TEST KITK830615CYTOMEGELISA STATK823805VARICELISA TEST KITK821967CHLAMYDELISA TEST KIT

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Related Devices (Code: LJB)

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.

K974552DIAMEDIX IS-MEASLES IGG TEST SYSTEMDiamedix Corp.K971620QUANTA LITE RUBEOLA (MEASLES) IGGInova Diagnostics, Inc.K922330BARTELS RUBEOLA IGG EIABaxter Diagnostics, Inc.K922335BARTELS RUBEOLA IGM EIABaxter Diagnostics, Inc.K910290VIRATEST-DIA(TM) MEASLES (RUBEOLA)Virus Reference Laboratory, Inc.K904083RUBEOLA IGM ELISA TESTGull Laboratories, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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