NON-REUSABLE UNIVERSAL NEBULIZER FILTE
K-Number: K823257 · 1982-12-09
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Device Summary
Frequently Asked Questions
What is the NON-REUSABLE UNIVERSAL NEBULIZER FILTE?
NON-REUSABLE UNIVERSAL NEBULIZER FILTE is a medical device that received FDA 510(k) clearance on 1982-12-09. The listed applicant is Ohio Medical Products. The 510(k) number is K823257.
When did NON-REUSABLE UNIVERSAL NEBULIZER FILTE receive FDA 510(k) clearance?
NON-REUSABLE UNIVERSAL NEBULIZER FILTE received FDA 510(k) clearance on 1982-12-09, under 510(k) number K823257.
Who is the listed applicant for NON-REUSABLE UNIVERSAL NEBULIZER FILTE?
The FDA 510(k) record lists Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-REUSABLE UNIVERSAL NEBULIZER FILTE?
The FDA product code for NON-REUSABLE UNIVERSAL NEBULIZER FILTE is CAH.
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 Ohio 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: CAH)
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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