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 pump, portable, aspiration (manual or powered)
510(k) Number K041199
Device Name MEDI-PUMP ASPIRATOR, MODEL 1615
Applicant
THOMAS INDUSTRIES
1419 ILLINOIS AVE.
SHEBOYGAN,  WI  53082 -0029
Applicant Contact DANIEL PFISTER
Correspondent
THOMAS INDUSTRIES
1419 ILLINOIS AVE.
SHEBOYGAN,  WI  53082 -0029
Correspondent Contact DANIEL PFISTER
Regulation Number878.4780
Classification Product Code
BTA  
Date Received05/07/2004
Decision Date 06/01/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-