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 K984040
Device Name BLOSSOM POWDERED LATEX EXAMINATION GLOVES
Applicant
Mexpo Intl., Inc.
2671 Mccone Ave.
Hayward,,  CA  94545
Applicant Contact TIM THAI
Correspondent
Mexpo Intl., Inc.
2671 Mccone Ave.
Hayward,,  CA  94545
Correspondent Contact TIM THAI
Regulation Number880.6250
Classification Product Code
LYY  
Date Received11/12/1998
Decision Date 01/13/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-