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 Unit, Cryosurgical, Accessories
510(k) Number K170810
Device Name CRYOFOS
Applicant
Cryofos Medical GmbH
Lammstrasse 21
Karlsruhe,  DE 76133
Applicant Contact Gerlinde Hornung-Stehling
Correspondent
Tenssource, LLC
724 Bald Cypress Place
Tampa,  FL  33614
Correspondent Contact Nick Stocks
Regulation Number878.4350
Classification Product Code
GEH  
Subsequent Product Code
MLY  
Date Received03/17/2017
Decision Date 09/27/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-