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 Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
510(k) Number K210836
Device Name InstruSafe Instrument Protection System
Applicant
Summitt Medical LLC
815 Vikings Pkwy, Suite 100
St. Paul,  MN  55121
Applicant Contact Debra Kridner
Correspondent
Summitt Medical LLC
815 Vikings Pkwy, Suite 100
St. Paul,  MN  55121
Correspondent Contact Debra Kridner
Regulation Number880.6850
Classification Product Code
KCT  
Date Received03/22/2021
Decision Date 11/30/2021
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-