I.P.P.B., DIS. W/MANIFOLD/NEBULIZER
K-Number: K760221 · 1976-08-03
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Device Summary
Frequently Asked Questions
What is the I.P.P.B., DIS. W/MANIFOLD/NEBULIZER?
I.P.P.B., DIS. W/MANIFOLD/NEBULIZER is a medical device that received FDA 510(k) clearance on 1976-08-03. The listed applicant is Manner Medical Products. The 510(k) number is K760221.
When did I.P.P.B., DIS. W/MANIFOLD/NEBULIZER receive FDA 510(k) clearance?
I.P.P.B., DIS. W/MANIFOLD/NEBULIZER received FDA 510(k) clearance on 1976-08-03, under 510(k) number K760221.
Who is the listed applicant for I.P.P.B., DIS. W/MANIFOLD/NEBULIZER?
The FDA 510(k) record lists Manner Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for I.P.P.B., DIS. W/MANIFOLD/NEBULIZER?
The FDA product code for I.P.P.B., DIS. W/MANIFOLD/NEBULIZER is CBO.
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 Manner Medical Products 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: CBO)
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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