MISTY OX LAMINAR DIFFUSER HUMIDIFIER
K-Number: K923754 · 1992-12-07
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Device Summary
Frequently Asked Questions
What is the MISTY OX LAMINAR DIFFUSER HUMIDIFIER?
MISTY OX LAMINAR DIFFUSER HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1992-12-07. The listed applicant is Medical Molding Corp. of America. The 510(k) number is K923754.
When did MISTY OX LAMINAR DIFFUSER HUMIDIFIER receive FDA 510(k) clearance?
MISTY OX LAMINAR DIFFUSER HUMIDIFIER received FDA 510(k) clearance on 1992-12-07, under 510(k) number K923754.
Who is the listed applicant for MISTY OX LAMINAR DIFFUSER HUMIDIFIER?
The FDA 510(k) record lists Medical Molding Corp. of America as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MISTY OX LAMINAR DIFFUSER HUMIDIFIER?
The FDA product code for MISTY OX LAMINAR DIFFUSER HUMIDIFIER is BTT.
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 Medical Molding Corp. of America 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: BTT)
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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