FDA 510(k) Applications Submitted by COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K083519 |
11/26/2008 |
AUTOSUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
| K091900 |
06/25/2009 |
ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
| K090419 |
02/18/2009 |
SILS STITCH ENDOSCOPIC SUTURING DEVICE |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
| K091869 |
06/23/2009 |
SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
| K082619 |
09/09/2008 |
SILS PORT, MODELS SILSPT5, SILSPT12 |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
| K082659 |
09/12/2008 |
MODIFIED ENDO STICH |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
| K081169 |
04/24/2008 |
AUTOSUTURE VERSAPORT PLUS BLADLESS TROCAR; BLADELESS TROCAR |
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES |
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