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 Hemostat
510(k) Number K881937
Device Name SURGICAL INSTRUMENTS
Applicant
Far East Intl. Trading Corp.
727 N. Broadway, Suite 101
Los Angeles,  CA  90012
Applicant Contact JULIA SUN
Correspondent
Far East Intl. Trading Corp.
727 N. Broadway, Suite 101
Los Angeles,  CA  90012
Correspondent Contact JULIA SUN
Regulation Number878.4800
Classification Product Code
HRQ  
Date Received05/09/1988
Decision Date 06/15/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-