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 K892781
Device Name ANTELOPE BRAND PATIENT EXAMINATION GLOVES
Applicant
Liaoning-Usa Corp.
123 W. Bellevue, Unit#4
Pasadena,  CA  91105
Applicant Contact DIANA BRYAN
Correspondent
Liaoning-Usa Corp.
123 W. Bellevue, Unit#4
Pasadena,  CA  91105
Correspondent Contact DIANA BRYAN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/11/1989
Decision Date 09/21/1989
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
-
-