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FDA 510(k)

I.P.P.B., DIS. W/MANIFOLD/NEBULIZER

K-Number: K760221 · 1976-08-03

Decision Date1976-08-03
Product CodeCBO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

I.P.P.B., DIS. W/MANIFOLD/NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Manner Medical Products. It received FDA 510(k) clearance on 1976-08-03 under 510(k) number K760221. The device is classified under product code CBO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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