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 Tape And Bandage, Adhesive
510(k) Number K870020
Device Name IV SECUREMENT DEVICE
Applicant
AVERY INTL.
FASSON MEDICAL PRODUCTS
7100 LINDSAY DRIVE
MENTOR,  OH  44060
Applicant Contact HOWARD T COOPER
Correspondent
AVERY INTL.
FASSON MEDICAL PRODUCTS
7100 LINDSAY DRIVE
MENTOR,  OH  44060
Correspondent Contact HOWARD T COOPER
Regulation Number880.5240
Classification Product Code
KGX  
Date Received01/02/1987
Decision Date 02/04/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-