VHS 820 Humidifier, Modification

FDA 510(k) K893034 · Bear Medical Systems, Inc.

Substantially Equivalent

510(k) numberK893034

Submission

Device name
VHS 820 Humidifier, Modification
Applicant
Bear Medical Systems, Inc.
Riverside, CA, US
Received
April 20, 1989
Decision date
July 14, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTT – Humidifier, Respiratory Gas, (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5450
Specialty
Anesthesiology

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Questions and answers

When was VHS 820 Humidifier, Modification cleared by the FDA?

VHS 820 Humidifier, Modification (K893034) received a 510(k) decision of Substantially Equivalent on July 14, 1989, 85 days after the submission was received.

What is the product code of K893034?

The FDA product code is BTT – Humidifier, Respiratory Gas, (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5450.