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 Garment, Protective, For Incontinence
510(k) Number K883894
Device Name DRIPRIDE PROVIDE SLIM
Applicant
Weyerhaeuser Co.
2101 L St. NW
Washington,  DC  20037
Applicant Contact HOWARD M HOLSTEIN
Correspondent
Weyerhaeuser Co.
2101 L St. NW
Washington,  DC  20037
Correspondent Contact HOWARD M HOLSTEIN
Regulation Number876.5920
Classification Product Code
EYQ  
Date Received09/14/1988
Decision Date 01/30/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-