• 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 K952895
Device Name CMS URETHRAL WARMER
Applicant
CRYOMEDICAL SCIENCES, INC.
1300 PICCARD DR.
ROCKVILLE,  MD  20850
Applicant Contact CLAUDE C CRAWFORD
Correspondent
CRYOMEDICAL SCIENCES, INC.
1300 PICCARD DR.
ROCKVILLE,  MD  20850
Correspondent Contact CLAUDE C CRAWFORD
Regulation Number878.4350
Classification Product Code
GEH  
Subsequent Product Code
KOE  
Date Received06/23/1995
Decision Date 10/24/1995
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
-
-