510(k) K952037

3 LPM OXYGEN CONCENTRATOR by Devilbiss Health Care, Inc. — Product Code CAW

K952037 is an FDA 510(k) premarket notification submitted by Devilbiss Health Care, Inc. for the device "3 LPM OXYGEN CONCENTRATOR". The FDA issued a decision of Substantially Equivalent on September 6, 1995. The device falls under product code CAW (Generator, Oxygen, Portable), a Class II device regulated under 21 CFR 868.5440. Devilbiss Health Care, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 6, 1995
Date Received
May 1, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Generator, Oxygen, Portable
Device Class
Class II
Regulation Number
868.5440
Review Panel
AN
Submission Type