• 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 K111138
Device Name THE PICC WAND (R) PEELABLE SAFETY INTRODUCER
Applicant
ACCESS SCIENTIFIC, INC.
12526 HIGH BLUFF DRIVE
SUITE 360
SAN DIEGO,  CA  92130
Applicant Contact ALBERT MISAJON
Correspondent
ACCESS SCIENTIFIC, INC.
12526 HIGH BLUFF DRIVE
SUITE 360
SAN DIEGO,  CA  92130
Correspondent Contact ALBERT MISAJON
Regulation Number870.1340
Classification Product Code
DYB  
Date Received04/22/2011
Decision Date 06/22/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-