• 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 K840754
Device Name MAXISHIELD INCONTINENCE CARE SYSTEM
Applicant
IPCO CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
IPCO CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number876.5920
Classification Product Code
EYQ  
Date Received02/23/1984
Decision Date 04/13/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-