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 Wrap, Sterilization
510(k) Number K202593
Device Name Turbett Instrument Pod
Applicant
Turbett Surgical, Inc.
125 Tech Park Dr.
Rochester,  NY  14625
Applicant Contact Rob Turbett
Correspondent
Fdc Services
8708 Capehart Cove
Austin,  TX  78733
Correspondent Contact David Furr
Regulation Number880.6850
Classification Product Code
FRG  
Date Received09/08/2020
Decision Date 05/19/2021
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
-
-