Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 Unit, Liquid-Oxygen, Portable
510(k) Number K853083
Device Name RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR
Applicant
HOME MEDICAL SUPPLY, INC.
300 N. 2ND ST.
CLEARFIELD,  PA  16830
Applicant Contact KENNETH STEWART
Correspondent
HOME MEDICAL SUPPLY, INC.
300 N. 2ND ST.
CLEARFIELD,  PA  16830
Correspondent Contact KENNETH STEWART
Regulation Number868.5655
Classification Product Code
BYJ  
Date Received07/23/1985
Decision Date 09/03/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-