• 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 Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K903610
Device Name O.R. TIP CLEANER
Applicant
Inman Liebelt Corp.
P.O. Box 171077
Arlington,  TX  76003
Applicant Contact CLAY WILSON
Correspondent
Inman Liebelt Corp.
P.O. Box 171077
Arlington,  TX  76003
Correspondent Contact CLAY WILSON
Regulation Number878.4400
Classification Product Code
GEI  
Date Received08/09/1990
Decision Date 10/19/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-