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 condenser, heat and moisture (artificial nose)
510(k) Number K902501
Device Name FLOCARE N
Applicant
FLOCARE MEDICAL
992 EAGLE SCHOOL RD.
SUITE 913
WAYNE,  PA  19087
Applicant Contact AL W KRAUS
Correspondent
FLOCARE MEDICAL
992 EAGLE SCHOOL RD.
SUITE 913
WAYNE,  PA  19087
Correspondent Contact AL W KRAUS
Regulation Number868.5375
Classification Product Code
BYD  
Date Received06/05/1990
Decision Date 07/02/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-