• 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 Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
510(k) Number K924083
Device Name 700/700-1
Applicant
CITICARE SYSTEMS, INC.
P.O. BOX 26556
MILWAUKEE,  WI  53226
Applicant Contact ALEX KAPLAN
Correspondent
CITICARE SYSTEMS, INC.
P.O. BOX 26556
MILWAUKEE,  WI  53226
Correspondent Contact ALEX KAPLAN
Regulation Number868.1400
Classification Product Code
CCK  
Date Received08/13/1992
Decision Date 03/10/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-