Model 590 Oxygen Concentrator

FDA 510(k) K895141 · Puritan Bennett Corp.

Substantially Equivalent

510(k) numberK895141

Submission

Device name
Model 590 Oxygen Concentrator
Applicant
Puritan Bennett Corp.
Overland Park, KS, US
Received
August 16, 1989
Decision date
October 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 Model 590 Oxygen Concentrator cleared by the FDA?

Model 590 Oxygen Concentrator (K895141) received a 510(k) decision of Substantially Equivalent on October 31, 1989, 76 days after the submission was received.

What is the product code of K895141?

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