Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PASSIVE WASTE GAS SCAVENGER, MODEL 14600

K-Number: K080039 · 2008-04-14

Decision Date2008-04-14
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PASSIVE WASTE GAS SCAVENGER, MODEL 14600 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 2008-04-14 under 510(k) number K080039. 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 PASSIVE WASTE GAS SCAVENGER, MODEL 14600?

PASSIVE WASTE GAS SCAVENGER, MODEL 14600 is a medical device that received FDA 510(k) clearance on 2008-04-14. The listed applicant is G. Dundas Co.,Inc.. The 510(k) number is K080039.

When did PASSIVE WASTE GAS SCAVENGER, MODEL 14600 receive FDA 510(k) clearance?

PASSIVE WASTE GAS SCAVENGER, MODEL 14600 received FDA 510(k) clearance on 2008-04-14, under 510(k) number K080039.

Who is the listed applicant for PASSIVE WASTE GAS SCAVENGER, MODEL 14600?

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 PASSIVE WASTE GAS SCAVENGER, MODEL 14600?

The FDA product code for PASSIVE WASTE GAS SCAVENGER, MODEL 14600 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑