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FDA 510(k)

PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C

K-Number: K041664 · 2004-07-29

Decision Date2004-07-29
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C is the device name listed in this FDA 510(k) record. The listed applicant is On Site Gas Systems, Inc.. It received FDA 510(k) clearance on 2004-07-29 under 510(k) number K041664. 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 PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C?

PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C is a medical device that received FDA 510(k) clearance on 2004-07-29. The listed applicant is On Site Gas Systems, Inc.. The 510(k) number is K041664.

When did PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C receive FDA 510(k) clearance?

PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C received FDA 510(k) clearance on 2004-07-29, under 510(k) number K041664.

Who is the listed applicant for PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C?

The FDA 510(k) record lists On Site Gas Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C?

The FDA product code for PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C 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 On Site Gas Systems, 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.

View all 9 devices →

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

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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