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 Wire, Guide, Catheter
510(k) Number K113162
Device Name SLIDEWIRETM(TRADEMARK PENDING)
Applicant
Acme-Monaco Corp.
75 Winchell Dr.
New Britain,  CT  06052
Applicant Contact BENJAMIN SWEENEY
Correspondent
Acme-Monaco Corp.
75 Winchell Dr.
New Britain,  CT  06052
Correspondent Contact BENJAMIN SWEENEY
Regulation Number870.1330
Classification Product Code
DQX  
Date Received10/26/2011
Decision Date 07/20/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-