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FDA 510(k)

NEBULIZER ADAPTER

K-Number: K772348 · 1978-01-03

ApplicantRespiratory Care, Inc.
Decision Date1978-01-03
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Care, Inc.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772348. 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 NEBULIZER ADAPTER?

NEBULIZER ADAPTER is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K772348.

When did NEBULIZER ADAPTER receive FDA 510(k) clearance?

NEBULIZER ADAPTER received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772348.

Who is the listed applicant for NEBULIZER ADAPTER?

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

What is the FDA product code for NEBULIZER ADAPTER?

The FDA product code for NEBULIZER ADAPTER is CAF.

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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.

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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.

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