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FDA 510(k)

QUANTA LITE MPO

K-Number: K955022 · 1996-03-19

ApplicantInova Diagnostics, Inc.
Decision Date1996-03-19
Product CodeMOB
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUANTA LITE MPO 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 1996-03-19 under 510(k) number K955022. The device is classified under product code MOB. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTA LITE MPO?

QUANTA LITE MPO is a medical device that received FDA 510(k) clearance on 1996-03-19. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K955022.

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

QUANTA LITE MPO received FDA 510(k) clearance on 1996-03-19, under 510(k) number K955022.

Who is the listed applicant for QUANTA LITE MPO?

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 MPO?

The FDA product code for QUANTA LITE MPO is MOB.

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Related Devices (Code: MOB)

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.

K261466Alegria Flash MPO; Alegria Flash PR3; Alegria Flash GBMZeus ScientificK243776Anti-Neutrophil Cytoplasmic Antibodies (Ethanol-Fixed); Anti-Neutrophil Cytoplasmic Antibodies (Formalin-Fixed)Zeus ScientificK172582EUROIMMUN IFA Granulocyte Mosaic™ EUROPattern and EUROIMMUN EUROPLUS Granulocyte Mosaic™ EUROPatternEuroimmun Us, Inc.K172461AESKUSLIDES ANCA Ethanol, AESKUSLIDES ANCA FormalinAesku.Diagnostics GmbH & Co. KGK173792EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM ImmunoassayPhadia ABK161258NOVA Lite DAPI ANCA Ethanol Kit, NOVA Lite DAPI ANCA Formalin KitInova Diagnostics, 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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