• 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 Bandage, Elastic
510(k) Number K770958
Device Name BANDAGE, UNIPRESS, CLARION
Applicant
Sherwood Medical Industries
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Sherwood Medical Industries
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.5075
Classification Product Code
FQM  
Date Received05/27/1977
Decision Date 06/14/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-