• 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 Clamp, Surgical, General & Plastic Surgery
510(k) Number K853583
Device Name MODERN MEDICAL PRODUCTS TOWEL CLAMP
Applicant
Modern Medical Products
3901 Macarthur Blvd.
Suite 211
Newport Beach,  CA  92660
Applicant Contact STEPHEN GEORGEVICH
Correspondent
Modern Medical Products
3901 Macarthur Blvd.
Suite 211
Newport Beach,  CA  92660
Correspondent Contact STEPHEN GEORGEVICH
Regulation Number878.4800
Classification Product Code
GDJ  
Date Received08/26/1985
Decision Date 09/16/1985
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
-
-