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 Container, I.V.
510(k) Number K854034
Device Name SNAP-LOCK ADDITIVE CAP #SL 300
Applicant
Williams Medical Co.
P.O. Box 1122
4868 Olinda St.
Yorba Linda,  CA  92686
Applicant Contact DANIEL J WILLIAMS
Correspondent
Williams Medical Co.
P.O. Box 1122
4868 Olinda St.
Yorba Linda,  CA  92686
Correspondent Contact DANIEL J WILLIAMS
Regulation Number880.5025
Classification Product Code
KPE  
Date Received10/01/1985
Decision Date 11/06/1985
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
-
-