WH150 ROOM HUMIDIFIER
K-Number: K871661 · 1987-06-15
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Device Summary
Frequently Asked Questions
What is the WH150 ROOM HUMIDIFIER?
WH150 ROOM HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1987-06-15. The listed applicant is Associated Mills, Inc.. The 510(k) number is K871661.
When did WH150 ROOM HUMIDIFIER receive FDA 510(k) clearance?
WH150 ROOM HUMIDIFIER received FDA 510(k) clearance on 1987-06-15, under 510(k) number K871661.
Who is the listed applicant for WH150 ROOM HUMIDIFIER?
The FDA 510(k) record lists Associated Mills, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WH150 ROOM HUMIDIFIER?
The FDA product code for WH150 ROOM HUMIDIFIER is KFZ.
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 Associated Mills, Inc. 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: KFZ)
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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