• 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 Syringe, Irrigating (Dental)
510(k) Number K911118
Device Name DTF-1000LL,DTF-1000
Applicant
Cp Medical
P.O. Box 5668
Huntington Beach,  CA  92615
Applicant Contact CARL GRODACH
Correspondent
Cp Medical
P.O. Box 5668
Huntington Beach,  CA  92615
Correspondent Contact CARL GRODACH
Regulation Number872.4565
Classification Product Code
EIB  
Date Received03/12/1991
Decision Date 11/20/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-