Keystone Concentrator, Model PV5L

FDA 510(k) K924152 · Devilbiss Health Care, Inc.

Substantially Equivalent

510(k) numberK924152

Submission

Device name
Keystone Concentrator, Model PV5L
Applicant
Devilbiss Health Care, Inc.
Somerset, PA, US
Received
August 18, 1992
Decision date
June 7, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 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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K9538155 LPM Oxygen ConcentratorCAW · Traditional 11/09/1995SE
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Questions and answers

When was Keystone Concentrator, Model PV5L cleared by the FDA?

Keystone Concentrator, Model PV5L (K924152) received a 510(k) decision of Substantially Equivalent on June 7, 1993, 293 days after the submission was received.

What is the product code of K924152?

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