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 Nebulizer (Direct Patient Interface)
510(k) Number K895231
Device Name CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER
Applicant
Hudson Oxygen Therapy Sales Co.
27711 Diaz St.
P.O. Box 66
Temecula,  CA  92390
Applicant Contact JORGE HAIDER
Correspondent
Hudson Oxygen Therapy Sales Co.
27711 Diaz St.
P.O. Box 66
Temecula,  CA  92390
Correspondent Contact JORGE HAIDER
Regulation Number868.5630
Classification Product Code
CAF  
Date Received08/22/1989
Decision Date 10/27/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-