SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER
K-Number: K862042 · 1986-06-05
Advertisement
Device Summary
Frequently Asked Questions
What is the SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER?
SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1986-06-05. The listed applicant is Associated Mills, Inc.. The 510(k) number is K862042.
When did SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER receive FDA 510(k) clearance?
SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER received FDA 510(k) clearance on 1986-06-05, under 510(k) number K862042.
Who is the listed applicant for SH20, SH30 & SH50 ULTRASONIC 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 SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER?
The FDA product code for SH20, SH30 & SH50 ULTRASONIC 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.
Advertisement