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 cart, emergency, cardiopulmonary (excluding equipment)
510(k) Number K840264
Device Name SERVO CART 170
Applicant
SIEMENS ELEMA AB
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SIEMENS ELEMA AB
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.6175
Classification Product Code
BZN  
Date Received01/23/1984
Decision Date 02/04/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-