Precision Medical Disposable Humidifier

FDA 510(k) K902970 · Precision Medical, Inc.

Substantially Equivalent

510(k) numberK902970

Submission

Device name
Precision Medical Disposable Humidifier
Applicant
Precision Medical, Inc.
Bath, PA, US
Received
July 6, 1990
Decision date
August 14, 1990
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 Precision Medical Disposable Humidifier cleared by the FDA?

Precision Medical Disposable Humidifier (K902970) received a 510(k) decision of Substantially Equivalent on August 14, 1990, 39 days after the submission was received.

What is the product code of K902970?

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