FDA 510(k) Applications Submitted by SURGRX, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K070165 |
01/18/2007 |
ENSEAL PTC TRIO |
SURGRX, INC. |
K050671 |
03/15/2005 |
ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM |
SURGRX, INC. |
K070896 |
04/02/2007 |
ENSEAL PTC TISSUE SEALING DEVICE |
SURGRX, INC. |
K081129 |
04/21/2008 |
ENSEAL POWERTIP,NSEAL-514D,-525D,-535D,-545D,-514RD,-525RD,-535RD,-545RD, ETRIO-314D,-325D,-335D,-345D, ENSEAL UNIVERSAL |
SURGRX, INC. |
K071728 |
06/25/2007 |
MODIFICATION TO: ENSEAL PTC TISSUE SEALING DEVICE |
SURGRX, INC. |
K072177 |
08/06/2007 |
ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM |
SURGRX, INC. |
K063097 |
10/10/2006 |
ENSEAL PTC TISSUE SEALING DEVICE |
SURGRX, INC. |
K043008 |
11/01/2004 |
SURGRX ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM |
SURGRX, INC. |
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