Covidien Lp, Formerly Registered AS United States
Covidien Lp, Formerly Registered AS United States holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2009.
Top product codes for Covidien Lp, Formerly Registered AS United States
Recent clearances by Covidien Lp, Formerly Registered AS United States
- K091869 — SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS
- K091900 — ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE
- K083519 — AUTOSUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS
- K090419 — SILS STITCH ENDOSCOPIC SUTURING DEVICE
- K082619 — SILS PORT, MODELS SILSPT5, SILSPT12
- K082659 — MODIFIED ENDO STICH
- K081169 — AUTOSUTURE VERSAPORT PLUS BLADLESS TROCAR; BLADELESS TROCAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.