• 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 Collector, Urine, (And Accessories) For Indwelling Catheter
510(k) Number K842257
Device Name CORPAK URINARY DRAINAGE BAG
Applicant
Corpak Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Corpak Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number876.5250
Classification Product Code
KNX  
Date Received06/07/1984
Decision Date 08/08/1984
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
-
-