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 Probe, Radiofrequency Lesion
510(k) Number K000073
Device Name MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
Applicant
MERCURY MEDICAL
160 SOUTH MAIN ST.
SUITE A
MIDDLETON,  MA  01949
Applicant Contact MATTHEW NEKOROSKI
Correspondent
MERCURY MEDICAL
160 SOUTH MAIN ST.
SUITE A
MIDDLETON,  MA  01949
Correspondent Contact MATTHEW NEKOROSKI
Regulation Number882.4725
Classification Product Code
GXI  
Date Received01/10/2000
Decision Date 03/01/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-