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FDA 510(k)

AVL BLOOD GAS INSTRUMENT MODEL 939

K-Number: K771147 · 1977-09-15

Decision Date1977-09-15
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AVL BLOOD GAS INSTRUMENT MODEL 939 is the device name listed in this FDA 510(k) record. The listed applicant is Jones Medical Instrument Co.. It received FDA 510(k) clearance on 1977-09-15 under 510(k) number K771147. 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 BLOOD GAS INSTRUMENT MODEL 939?

AVL BLOOD GAS INSTRUMENT MODEL 939 is a medical device that received FDA 510(k) clearance on 1977-09-15. The listed applicant is Jones Medical Instrument Co.. The 510(k) number is K771147.

When did AVL BLOOD GAS INSTRUMENT MODEL 939 receive FDA 510(k) clearance?

AVL BLOOD GAS INSTRUMENT MODEL 939 received FDA 510(k) clearance on 1977-09-15, under 510(k) number K771147.

Who is the listed applicant for AVL BLOOD GAS INSTRUMENT MODEL 939?

The FDA 510(k) record lists Jones Medical Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVL BLOOD GAS INSTRUMENT MODEL 939?

The FDA product code for AVL BLOOD GAS INSTRUMENT MODEL 939 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.

Other records listing Jones Medical Instrument Co. 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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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