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FDA 510(k)

MINIOX IA OXYGEN ANALYZER

K-Number: K935370 · 1994-08-02

Decision Date1994-08-02
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MINIOX IA OXYGEN ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Minesafety Appliances Co.. It received FDA 510(k) clearance on 1994-08-02 under 510(k) number K935370. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIOX IA OXYGEN ANALYZER?

MINIOX IA OXYGEN ANALYZER is a medical device that received FDA 510(k) clearance on 1994-08-02. The listed applicant is Minesafety Appliances Co.. The 510(k) number is K935370.

When did MINIOX IA OXYGEN ANALYZER receive FDA 510(k) clearance?

MINIOX IA OXYGEN ANALYZER received FDA 510(k) clearance on 1994-08-02, under 510(k) number K935370.

Who is the listed applicant for MINIOX IA OXYGEN ANALYZER?

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

What is the FDA product code for MINIOX IA OXYGEN ANALYZER?

The FDA product code for MINIOX IA OXYGEN ANALYZER is CAW.

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 Minesafety Appliances 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: CAW)

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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