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 Instruments, Surgical, Cardiovascular
510(k) Number K760645
Device Name CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP
Applicant
Pilling Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Pilling Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4500
Classification Product Code
DWS  
Date Received09/15/1976
Decision Date 09/21/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-