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FDA 510(k)

OXYGEN CONTROLLER MODEL 145

K-Number: K812038 · 1981-07-21

ApplicantMedix Medical Electronics (U.S.A.), Inc.
Decision Date1981-07-21
Product Code
DecisionSubstantially Equivalent

Device Summary

OXYGEN CONTROLLER MODEL 145 is the device name listed in this FDA 510(k) record. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. It received FDA 510(k) clearance on 1981-07-21 under 510(k) number K812038. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYGEN CONTROLLER MODEL 145?

OXYGEN CONTROLLER MODEL 145 is a medical device that received FDA 510(k) clearance on 1981-07-21. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. The 510(k) number is K812038.

When did OXYGEN CONTROLLER MODEL 145 receive FDA 510(k) clearance?

OXYGEN CONTROLLER MODEL 145 received FDA 510(k) clearance on 1981-07-21, under 510(k) number K812038.

Who is the listed applicant for OXYGEN CONTROLLER MODEL 145?

The FDA 510(k) record lists Medix Medical Electronics (U.S.A.), Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Medix Medical Electronics (U.S.A.), Inc. 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.

K861040ENTERNAL INFUSER MULTIPUMP 203K861001PARENTERAL INFUSER MEDIPUMP 204K853393INSULIN PUMP INSUMAT 229K852433INFUSAFE 205 CATOLOG NO. 205.000K813562SYRINGE DRIVER 209K812039SPIROMETER 210/211

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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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