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)

56 SERIES JET NEBULIZER

K-Number: K021443 · 2002-10-21

Decision Date2002-10-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

56 SERIES JET NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Project Marketing. It received FDA 510(k) clearance on 2002-10-21 under 510(k) number K021443. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 56 SERIES JET NEBULIZER?

56 SERIES JET NEBULIZER is a medical device that received FDA 510(k) clearance on 2002-10-21. The listed applicant is Project Marketing. The 510(k) number is K021443.

When did 56 SERIES JET NEBULIZER receive FDA 510(k) clearance?

56 SERIES JET NEBULIZER received FDA 510(k) clearance on 2002-10-21, under 510(k) number K021443.

Who is the listed applicant for 56 SERIES JET NEBULIZER?

The FDA 510(k) record lists Project Marketing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 56 SERIES JET NEBULIZER?

The FDA product code for 56 SERIES JET NEBULIZER is CAF.

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 Project Marketing 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: CAF)

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.

↑