H-3000 Oxygen Concentrator

FDA 510(k) K890150 · Healthdyne, Inc.

Substantially Equivalent

510(k) numberK890150

Submission

Device name
H-3000 Oxygen Concentrator
Applicant
Healthdyne, Inc.
Marietta, GA, US
Received
January 13, 1989
Decision date
January 31, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAW – Generator, Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5440
Specialty
Anesthesiology

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Questions and answers

When was H-3000 Oxygen Concentrator cleared by the FDA?

H-3000 Oxygen Concentrator (K890150) received a 510(k) decision of Substantially Equivalent on January 31, 1989, 18 days after the submission was received.

What is the product code of K890150?

The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.