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, Conduction, Anesthetic
510(k) Number K001717
Device Name MICOR CONDUCTION CATHETER
Applicant
Micor, Inc.
2855 Oxford Blvd.
Allison Park,  PA  15101
Applicant Contact JEREMIAH COSTELLO
Correspondent
Micor, Inc.
2855 Oxford Blvd.
Allison Park,  PA  15101
Correspondent Contact JEREMIAH COSTELLO
Regulation Number868.5120
Classification Product Code
BSO  
Date Received06/05/2000
Decision Date 09/20/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-