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FDA 510(k)

MODEL PUP II AND MINI-NEBULIZER

K-Number: K827291 · 1982-04-23

ApplicantBiermar AG
Decision Date1982-04-23
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL PUP II AND MINI-NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Biermar AG. It received FDA 510(k) clearance on 1982-04-23 under 510(k) number K827291. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL PUP II AND MINI-NEBULIZER?

MODEL PUP II AND MINI-NEBULIZER is a medical device that received FDA 510(k) clearance on 1982-04-23. The listed applicant is Biermar AG. The 510(k) number is K827291.

When did MODEL PUP II AND MINI-NEBULIZER receive FDA 510(k) clearance?

MODEL PUP II AND MINI-NEBULIZER received FDA 510(k) clearance on 1982-04-23, under 510(k) number K827291.

Who is the listed applicant for MODEL PUP II AND MINI-NEBULIZER?

The FDA 510(k) record lists Biermar AG as the applicant. This does not by itself establish the device manufacturer.

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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

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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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