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 Ventilator, Continuous, Facility Use
510(k) Number K893786
Device Name SERVO ANESTHESIA CIRCLE 985
Applicant
SIEMENS LIFE SUPPORT SYSTEMS
2360 N. PALMER DR.
SCHAUMBURG,  IL  60173
Applicant Contact ELLEN FARNEY
Correspondent
SIEMENS LIFE SUPPORT SYSTEMS
2360 N. PALMER DR.
SCHAUMBURG,  IL  60173
Correspondent Contact ELLEN FARNEY
Regulation Number868.5895
Classification Product Code
CBK  
Date Received05/22/1989
Decision Date 09/22/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-