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)

INHALATION OPERATED NEBULIZER CODE

K-Number: K791218 · 1979-07-30

Decision Date1979-07-30
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INHALATION OPERATED NEBULIZER CODE is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791218. 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 INHALATION OPERATED NEBULIZER CODE?

INHALATION OPERATED NEBULIZER CODE is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K791218.

When did INHALATION OPERATED NEBULIZER CODE receive FDA 510(k) clearance?

INHALATION OPERATED NEBULIZER CODE received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791218.

Who is the listed applicant for INHALATION OPERATED NEBULIZER CODE?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INHALATION OPERATED NEBULIZER CODE?

The FDA product code for INHALATION OPERATED NEBULIZER CODE 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 Travenol Laboratories, S.A. 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 206 devices →

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.

↑