BEAR VH-820 HUMIDIFIER
K-Number: K873634 · 1987-12-02
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Device Summary
Frequently Asked Questions
What is the BEAR VH-820 HUMIDIFIER?
BEAR VH-820 HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1987-12-02. The listed applicant is Bear Medical Systems, Inc.. The 510(k) number is K873634.
When did BEAR VH-820 HUMIDIFIER receive FDA 510(k) clearance?
BEAR VH-820 HUMIDIFIER received FDA 510(k) clearance on 1987-12-02, under 510(k) number K873634.
Who is the listed applicant for BEAR VH-820 HUMIDIFIER?
The FDA 510(k) record lists Bear Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEAR VH-820 HUMIDIFIER?
The FDA product code for BEAR VH-820 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 Bear Medical Systems, 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: 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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