• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Generator, Oxygen, Portable
510(k) Number K071397
FOIA Releasable 510(k) K071397
Device Name DEVILBISS 5 LITER COMPACT OXYGEN CONCENTRATOR, MODEL 525 SERIES
Applicant
SUNRISE MEDICAL
100 DEVILBISS DR.
SOMERSET,  PA  15501
Applicant Contact JOSEPH E OLSAVSKY
Correspondent
SUNRISE MEDICAL
100 DEVILBISS DR.
SOMERSET,  PA  15501
Correspondent Contact JOSEPH E OLSAVSKY
Regulation Number868.5440
Classification Product Code
CAW  
Date Received05/21/2007
Decision Date 10/01/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
Recalls CDRH Recalls
-
-