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FDA 510(k)

ELECTROLYTE PO2 FOR OXYGEN ELECTRODES

K-Number: K831024 · 1983-06-16

Decision Date1983-06-16
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROLYTE PO2 FOR OXYGEN ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1983-06-16 under 510(k) number K831024. 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 ELECTROLYTE PO2 FOR OXYGEN ELECTRODES?

ELECTROLYTE PO2 FOR OXYGEN ELECTRODES is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K831024.

When did ELECTROLYTE PO2 FOR OXYGEN ELECTRODES receive FDA 510(k) clearance?

ELECTROLYTE PO2 FOR OXYGEN ELECTRODES received FDA 510(k) clearance on 1983-06-16, under 510(k) number K831024.

Who is the listed applicant for ELECTROLYTE PO2 FOR OXYGEN ELECTRODES?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROLYTE PO2 FOR OXYGEN ELECTRODES?

The FDA product code for ELECTROLYTE PO2 FOR OXYGEN ELECTRODES 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 Fisher Scientific Co., LLC 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: 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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