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 sleeve, limb, compressible
510(k) Number K934639
Device Name JOBST ATHROMBIC PUMP - SYSTEM 2500
Applicant
JOBST INSTITUTE, INC.
P.O. BOX 471048
CHARLOTTE,  NC  28247 -1048
Applicant Contact KENNETH M BOLAM
Correspondent
JOBST INSTITUTE, INC.
P.O. BOX 471048
CHARLOTTE,  NC  28247 -1048
Correspondent Contact KENNETH M BOLAM
Regulation Number870.5800
Classification Product Code
JOW  
Date Received09/29/1993
Decision Date 02/09/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-