Surgrx, Inc.
Surgrx, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2008.
Top product codes for Surgrx, Inc.
Recent clearances by Surgrx, Inc.
- K081129 — ENSEAL POWERTIP,NSEAL-514D,-525D,-535D,-545D,-514RD,-525RD,-535RD,-545RD, ETRIO-314D,-325D,-335D,-345D, ENSEAL UNIVERSAL
- K072493 — ENSEAL TISSUE SEALING DEVICE
- K072177 — ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM
- K071728 — MODIFICATION TO: ENSEAL PTC TISSUE SEALING DEVICE
- K070896 — ENSEAL PTC TISSUE SEALING DEVICE
- K070165 — ENSEAL PTC TRIO
- K062949 — ENSEAL PTC TISSUE SEATING SEALING DEVICE
- K063097 — ENSEAL PTC TISSUE SEALING DEVICE
- K061526 — ENSEAL PTC TISSUE SEALING DEVICE
- K050671 — ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM
- K043008 — SURGRX ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM
- K031133 — SURGRX ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM INCLUDING THE ENSEAL CONTROLLER ADAPTER, ENSEAL OPEN AND LAPAROSCOPIS
Data sourced from openFDA. This site is unofficial and independent of the FDA.