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 K954703
Device Name MEDI-FRIG
Applicant
Ellman Intl., Inc.
30 Northport Rd.
Sound Beach,  NY  11789 -1734
Applicant Contact RICHARD C LANZILLOTTO
Correspondent
Ellman Intl., Inc.
30 Northport Rd.
Sound Beach,  NY  11789 -1734
Correspondent Contact RICHARD C LANZILLOTTO
Regulation Number878.4350
Classification Product Code
GEH  
Date Received10/12/1995
Decision Date 02/08/1996
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
Predetermined Change
Control Plan Authorized		 No
-
-