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FDA 510(k)

AVL 9181 ELECTROLYTE ANALYZER

K-Number: K972673 · 1997-08-20

ApplicantAvl Scientific Corp.
Decision Date1997-08-20
Product CodeJFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AVL 9181 ELECTROLYTE 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 1997-08-20 under 510(k) number K972673. The device is classified under product code JFP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVL 9181 ELECTROLYTE ANALYZER?

AVL 9181 ELECTROLYTE ANALYZER is a medical device that received FDA 510(k) clearance on 1997-08-20. The listed applicant is Avl Scientific Corp.. The 510(k) number is K972673.

When did AVL 9181 ELECTROLYTE ANALYZER receive FDA 510(k) clearance?

AVL 9181 ELECTROLYTE ANALYZER received FDA 510(k) clearance on 1997-08-20, under 510(k) number K972673.

Who is the listed applicant for AVL 9181 ELECTROLYTE 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 9181 ELECTROLYTE ANALYZER?

The FDA product code for AVL 9181 ELECTROLYTE ANALYZER is JFP.

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Other records listing Avl Scientific Corp. 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.

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Related Devices (Code: JFP)

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K230300i-STAT CG8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K191360i-STAT CHEM8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K191626Stat Profile Prime ES Comp Plus Analyzer SystemNova Biomedical CorporationK152327EasyLyte Na/K/Cl/Ca AnalyzerMedica CorporationK984299AVL OPTI CRITICAL CARE ANALYZERAvl Scientific Corp.K963694EASYLYTE CALCIUM/CHLORIDE ANALYZERMedica Corp.

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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