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 K212814
Device Name C2 CryoBalloon Ablation System
Applicant
Pentax of America, Inc.
303 Convention Way, Suite 1
Redwood, Ca,  CA  94063
Applicant Contact William Goeller
Correspondent
Pentax of America, Inc.
303 Convention Way, Suite 1
Redwood, Ca,  CA  94063
Correspondent Contact William Goeller
Regulation Number878.4350
Classification Product Code
GEH  
Date Received09/03/2021
Decision Date 11/29/2021
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
-
-