Portable Oxygen Concentrator, Model RS-00400

FDA 510(k) K073242 · Delphi Medical Systems

Substantially Equivalent

510(k) numberK073242

Submission

Device name
Portable Oxygen Concentrator, Model RS-00400
Applicant
Delphi Medical Systems
Troy, MI, US
Received
November 19, 2007
Decision date
January 3, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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 Portable Oxygen Concentrator, Model RS-00400 cleared by the FDA?

Portable Oxygen Concentrator, Model RS-00400 (K073242) received a 510(k) decision of Substantially Equivalent on January 3, 2008, 45 days after the submission was received.

What is the product code of K073242?

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