• 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 electrode measurement, blood-gases (pco2, po2) and blood ph
510(k) Number K002290
Device Name ABL-700 SERIES, MODEL ABL 7XX (VARIOUS MODELS)
Applicant
RADIOMETER MEDICAL A/S
AKANDEVEJ 21
BRONSHOJ,  DK DK-2700
Applicant Contact KIRSTEN RONO
Correspondent
RADIOMETER MEDICAL A/S
AKANDEVEJ 21
BRONSHOJ,  DK DK-2700
Correspondent Contact KIRSTEN RONO
Regulation Number862.1120
Classification Product Code
CHL  
Subsequent Product Codes
CEM   CGA   CGZ   CIG   GKF  
JFP   JGS   KHP  
Date Received07/27/2000
Decision Date 09/13/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-