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 Bedding, Disposable, Medical
510(k) Number K871725
Device Name DRIPRIDE DISPOSABLE UNDERPADS
Applicant
Weyerhaeuser Co.
Tacoma,  WA  98477
Applicant Contact RAIMO K RAHKONEN
Correspondent
Weyerhaeuser Co.
Tacoma,  WA  98477
Correspondent Contact RAIMO K RAHKONEN
Regulation Number880.6060
Classification Product Code
KME  
Date Received05/04/1987
Decision Date 05/15/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-