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 K980456
Device Name JOBST ATHROMBIC PUMP SYSTEM 2600
Applicant
Jobst A Beiersdorf Co.
5825 Carnegie Blvd.
Charlotte,  NC  28209
Applicant Contact KENNETH M BOLAM
Correspondent
Jobst A Beiersdorf Co.
5825 Carnegie Blvd.
Charlotte,  NC  28209
Correspondent Contact KENNETH M BOLAM
Regulation Number870.5800
Classification Product Code
JOW  
Date Received02/05/1998
Decision Date 05/05/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-