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FDA 510(k)

56 SERIES AEROSOL GENERATOR

K-Number: K980074 · 1998-06-12

ApplicantProject Marketing
Decision Date1998-06-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

56 SERIES AEROSOL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Project Marketing. It received FDA 510(k) clearance on 1998-06-12 under 510(k) number K980074. 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 AEROSOL GENERATOR?

56 SERIES AEROSOL GENERATOR is a medical device that received FDA 510(k) clearance on 1998-06-12. The listed applicant is Project Marketing. The 510(k) number is K980074.

When did 56 SERIES AEROSOL GENERATOR receive FDA 510(k) clearance?

56 SERIES AEROSOL GENERATOR received FDA 510(k) clearance on 1998-06-12, under 510(k) number K980074.

Who is the listed applicant for 56 SERIES AEROSOL GENERATOR?

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 AEROSOL GENERATOR?

The FDA product code for 56 SERIES AEROSOL GENERATOR is CAF.

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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.

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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.

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Official Source

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