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 clip, aneurysm
510(k) Number K844352
Device Name SUNDT-KEES REINFORCING ANEURYSM CLIP
Applicant
KEES SURGICAL SPECIALTY CO., INC.
104 NORTH ST.
WILDER,  KY  41071
Applicant Contact GEORGE KEES
Correspondent
KEES SURGICAL SPECIALTY CO., INC.
104 NORTH ST.
WILDER,  KY  41071
Correspondent Contact GEORGE KEES
Regulation Number882.5200
Classification Product Code
HCH  
Date Received11/09/1984
Decision Date 01/24/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-