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 Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
510(k) Number K080793
Device Name FIRMGRIP
Applicant
Flexicath , Ltd.
120 Yigal Alon St., Suite 107
Tel Aviv,  IL 67443
Applicant Contact TALI HAZAN
Correspondent
Flexicath , Ltd.
120 Yigal Alon St., Suite 107
Tel Aviv,  IL 67443
Correspondent Contact TALI HAZAN
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received03/20/2008
Decision Date 10/16/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-