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 tray, surgical, instrument
510(k) Number K944025
Device Name SURGICAL INSTRUMENT TRAY
Applicant
RILEY MEDICAL, INC.
49 PLAIN ST.
NORTH ATTLEBORO,  MA  02760
Applicant Contact DIANE E MINEAR
Correspondent
RILEY MEDICAL, INC.
49 PLAIN ST.
NORTH ATTLEBORO,  MA  02760
Correspondent Contact DIANE E MINEAR
Regulation Number878.4800
Classification Product Code
FSM  
Date Received08/17/1994
Decision Date 11/22/1994
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
-
-