• 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 Vinyl Patient Examination Glove
510(k) Number K030148
Device Name DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES WHITE COLOR
Applicant
SHANGHAI PALOMAR MOUNTAIN INDUSTRIES, INC.
#1 BIYU RD., CANGQIAO TOWNSHIP
SONGJIANG SHANGHAI,  CN 201600
Applicant Contact DANNY WANG
Correspondent
SHANGHAI PALOMAR MOUNTAIN INDUSTRIES, INC.
#1 BIYU RD., CANGQIAO TOWNSHIP
SONGJIANG SHANGHAI,  CN 201600
Correspondent Contact DANNY WANG
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received01/15/2003
Decision Date 02/19/2003
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
-
-