FDA 510(k) Applications Submitted by HYDROCISION, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020688 |
03/04/2002 |
HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR |
HYDROCISION, INC. |
| K991383 |
04/21/1999 |
HYDROCISION DEBDRIDEMENT SYSTEM |
HYDROCISION, INC. |
| K011612 |
05/25/2001 |
MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM |
HYDROCISION, INC. |
| K021813 |
06/03/2002 |
HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM |
HYDROCISION, INC. |
| K032529 |
08/15/2003 |
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310 |
HYDROCISION, INC. |
| K002764 |
09/05/2000 |
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR |
HYDROCISION, INC. |
| K993009 |
09/07/1999 |
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY |
HYDROCISION, INC. |
| K041233 |
05/10/2004 |
ARTHROJET XT |
HYDROCISION, INC. |
| K982266 |
06/29/1998 |
HYDROCISION ARTHROJET SYSTEM |
HYDROCISION, INC. |
| K200729 |
03/20/2020 |
HydroCision SpineJet System |
HydroCision, Inc. |
| K190804 |
03/29/2019 |
HydroCision TenJet Device |
HydroCision, Inc. |
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