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FDA 510(k)

AVL OMNI MODULAR ANALYZER

K-Number: K990092 · 1999-01-29

ApplicantAvl Scientific Corp.
Decision Date1999-01-29
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AVL OMNI MODULAR ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Avl Scientific Corp.. It received FDA 510(k) clearance on 1999-01-29 under 510(k) number K990092. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVL OMNI MODULAR ANALYZER?

AVL OMNI MODULAR ANALYZER is a medical device that received FDA 510(k) clearance on 1999-01-29. The listed applicant is Avl Scientific Corp.. The 510(k) number is K990092.

When did AVL OMNI MODULAR ANALYZER receive FDA 510(k) clearance?

AVL OMNI MODULAR ANALYZER received FDA 510(k) clearance on 1999-01-29, under 510(k) number K990092.

Who is the listed applicant for AVL OMNI MODULAR ANALYZER?

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

What is the FDA product code for AVL OMNI MODULAR ANALYZER?

The FDA product code for AVL OMNI MODULAR ANALYZER is CHL.

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Other records listing Avl Scientific Corp. as applicant

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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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