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FDA 510(k)

QUANTA LITE ACA SCREEN

K-Number: K923320 · 1992-09-28

ApplicantInova Diagnostics, Inc.
Decision Date1992-09-28
Product CodeMID
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUANTA LITE ACA SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Inova Diagnostics, Inc.. It received FDA 510(k) clearance on 1992-09-28 under 510(k) number K923320. The device is classified under product code MID. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTA LITE ACA SCREEN?

QUANTA LITE ACA SCREEN is a medical device that received FDA 510(k) clearance on 1992-09-28. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K923320.

When did QUANTA LITE ACA SCREEN receive FDA 510(k) clearance?

QUANTA LITE ACA SCREEN received FDA 510(k) clearance on 1992-09-28, under 510(k) number K923320.

Who is the listed applicant for QUANTA LITE ACA SCREEN?

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

What is the FDA product code for QUANTA LITE ACA SCREEN?

The FDA product code for QUANTA LITE ACA SCREEN is MID.

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Other records listing Inova Diagnostics, Inc. as applicant

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Related Devices (Code: MID)

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.

K223093Aptiva APS IgG Reagent; Aptiva APS IgM ReagentInova Diagnostics, Inc.K131821ELIA(TM) CARDIOLIPIN IGA IMMUNOASSAYPhadia US, Inc.K130528BIOPLEX 2200 APLS IGMBio-Rad LaboratoriesK120817QUANTA FLASH ACL LGA, QUANTA FLASH B2GP1 IGAInova Diagnostics, Inc.K113020IMMULISA ENHANCED (TM) CARDIOLIPIN IGA, IGG, IGM AND IGA/IGG/IGM ANTIBODY (ACA) ELISASImmco Diagnostics, Inc.K103834BIOPLEX 2200 APLS IGG AND IGA KIT AND CALIBRATOR AND CONTROL SETSBio-Rad Laboratories

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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