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FDA 510(k)

ACTIVE WASTE GAS SCAVENGER

K-Number: K110930 · 2011-06-23

Decision Date2011-06-23
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACTIVE WASTE GAS SCAVENGER is the device name listed in this FDA 510(k) record. The listed applicant is G. Dundas Co.,Inc.. It received FDA 510(k) clearance on 2011-06-23 under 510(k) number K110930. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIVE WASTE GAS SCAVENGER?

ACTIVE WASTE GAS SCAVENGER is a medical device that received FDA 510(k) clearance on 2011-06-23. The listed applicant is G. Dundas Co.,Inc.. The 510(k) number is K110930.

When did ACTIVE WASTE GAS SCAVENGER receive FDA 510(k) clearance?

ACTIVE WASTE GAS SCAVENGER received FDA 510(k) clearance on 2011-06-23, under 510(k) number K110930.

Who is the listed applicant for ACTIVE WASTE GAS SCAVENGER?

The FDA 510(k) record lists G. Dundas Co.,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTIVE WASTE GAS SCAVENGER?

The FDA product code for ACTIVE WASTE GAS SCAVENGER is CBN.

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 G. Dundas Co.,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.

Related Devices (Code: CBN)

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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