HEATED NEBULIZER
K-Number: K781542 · 1978-10-10
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Device Summary
Frequently Asked Questions
What is the HEATED NEBULIZER?
HEATED NEBULIZER is a medical device that received FDA 510(k) clearance on 1978-10-10. The listed applicant is Chemetron Medical Products, Inc.. The 510(k) number is K781542.
When did HEATED NEBULIZER receive FDA 510(k) clearance?
HEATED NEBULIZER received FDA 510(k) clearance on 1978-10-10, under 510(k) number K781542.
Who is the listed applicant for HEATED NEBULIZER?
The FDA 510(k) record lists Chemetron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEATED NEBULIZER?
The FDA product code for HEATED 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 Chemetron Medical Products, 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: 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.
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