Puritan-Bennett Aeris 590 Oxygen Concentrator with Oci

FDA 510(k) K993088 · Puritan Bennett Corp.

Substantially Equivalent

510(k) numberK993088

Submission

Device name
Puritan-Bennett Aeris 590 Oxygen Concentrator with Oci
Applicant
Puritan Bennett Corp.
Carlsbad, CA, US
Received
September 16, 1999
Decision date
October 8, 1999
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

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 Puritan-Bennett Aeris 590 Oxygen Concentrator with Oci cleared by the FDA?

Puritan-Bennett Aeris 590 Oxygen Concentrator with Oci (K993088) received a 510(k) decision of Substantially Equivalent on October 8, 1999, 22 days after the submission was received.

What is the product code of K993088?

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