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FDA 510(k)

INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853

K-Number: K963042 · 1996-11-01

Decision Date1996-11-01
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853 is the device name listed in this FDA 510(k) record. The listed applicant is Sim Italia S.R.L.. It received FDA 510(k) clearance on 1996-11-01 under 510(k) number K963042. 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 INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853?

INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853 is a medical device that received FDA 510(k) clearance on 1996-11-01. The listed applicant is Sim Italia S.R.L.. The 510(k) number is K963042.

When did INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853 receive FDA 510(k) clearance?

INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853 received FDA 510(k) clearance on 1996-11-01, under 510(k) number K963042.

Who is the listed applicant for INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853?

The FDA 510(k) record lists Sim Italia S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853?

The FDA product code for INNOSAN TRAVELAIR S PORTABLE OXYGEN CONCENTRATOR, CODE NO. M407001853 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 Sim Italia S.R.L. 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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