• 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 Cotton, Roll
510(k) Number K810830
Device Name HOYT COTTON ROLLS
Applicant
Hoyt Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Hoyt Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number872.6050
Classification Product Code
EFN  
Date Received03/25/1981
Decision Date 04/14/1981
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
-
-