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FDA 510(k)

MISTY OX LAMINAR DIFFUSER HUMIDIFIER

K-Number: K923754 · 1992-12-07

Decision Date1992-12-07
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MISTY OX LAMINAR DIFFUSER HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Molding Corp. of America. It received FDA 510(k) clearance on 1992-12-07 under 510(k) number K923754. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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

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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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