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FDA 510(k)

AVL MODEL 940 AUTOMATIC PH/BLOOD GAS

K-Number: K792230 · 1979-12-31

ApplicantGauntlet Technology Corp.
Decision Date1979-12-31
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AVL MODEL 940 AUTOMATIC PH/BLOOD GAS is the device name listed in this FDA 510(k) record. The listed applicant is Gauntlet Technology Corp.. It received FDA 510(k) clearance on 1979-12-31 under 510(k) number K792230. 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 MODEL 940 AUTOMATIC PH/BLOOD GAS?

AVL MODEL 940 AUTOMATIC PH/BLOOD GAS is a medical device that received FDA 510(k) clearance on 1979-12-31. The listed applicant is Gauntlet Technology Corp.. The 510(k) number is K792230.

When did AVL MODEL 940 AUTOMATIC PH/BLOOD GAS receive FDA 510(k) clearance?

AVL MODEL 940 AUTOMATIC PH/BLOOD GAS received FDA 510(k) clearance on 1979-12-31, under 510(k) number K792230.

Who is the listed applicant for AVL MODEL 940 AUTOMATIC PH/BLOOD GAS?

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

What is the FDA product code for AVL MODEL 940 AUTOMATIC PH/BLOOD GAS?

The FDA product code for AVL MODEL 940 AUTOMATIC PH/BLOOD GAS is CHL.

Related Clinical Trials

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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Other records listing Gauntlet Technology 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.

K801011AVL #980 ELECTROLYTE ANALYZER

Related Devices (Code: CHL)

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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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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