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 Introducer, Catheter
510(k) Number K050015
Device Name MODIFIED ACUMEN SHEATH, MODEL TTWO767
Applicant
Acumen Medical, Inc.
1400 Terra Bella Blvd.
Suite A
Mountain View,  CA  94043
Applicant Contact Marybeth Gamber
Correspondent
Acumen Medical, Inc.
1400 Terra Bella Blvd.
Suite A
Mountain View,  CA  94043
Correspondent Contact Marybeth Gamber
Regulation Number870.1340
Classification Product Code
DYB  
Date Received01/04/2005
Decision Date 02/03/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-