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 Latex Patient Examination Glove
510(k) Number K891738
Device Name PERFECT TOUCH PATIENT EXAM GLOVES (LATEX)
Applicant
Young Innovations, LLC Dba Plak Smacker
3741 Merced Dr., Unit E & F
Riverside,  CA  92503
Applicant Contact JOHN TAPOCIK
Correspondent
Young Innovations, LLC Dba Plak Smacker
3741 Merced Dr., Unit E & F
Riverside,  CA  92503
Correspondent Contact JOHN TAPOCIK
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/22/1989
Decision Date 04/26/1989
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
-
-