Product code NRY— Cardiovascular
EMBOTRAP III Revascularization Device
- Classification name
- Catheter, Thrombus Retriever
- Device class
- Class 2
- Regulation
- 21 CFR 870.1250
- Advisory panel
- Cardiovascular
- Total cleared
- 117
- First cleared
- Most recent
Clearances under product code NRY — page 2
101–117 of 117- K122478 — MODIFIED TREVO RETRIEVER
- K120961 — TREVO RETRIEVER
- K113455 — SOLITAIRE FR REVASCULARIZATION DEVICE
- K113163 — PENUMBRA SYSTEM MAX
- K093610 — MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153
- K100769 — PENUMBRA SYSTEM SEPARATOR FLEX (026,032,041,054), MODELS PSF026, PSF032, PSF041, PSF054
- K090752 — PENUMBRA SYSTEM (PENNUMBRA REPERFUSION CATHETER 054), MODEL PSC054; (PENUMBRA SEPARATOR 054), MODEL PSS054
- K090085 — MERCI RETRIEVER, MODELS 90050, 90060, 90066, 90070, 90110, 90111, 90112, 90113
- K082034 — MODIFICATION TO MERCI RETRIEVER
- K081305 — MERCI RETRIEVER
- K072718 — PENUMBRA SYSTEM
- K071172 — MODIFIED MERCI RETRIEVER, MODEL 90060
- K070521 — MODIFIED MERCY RETRIEVER, MODEL 90070
- K063774 — MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6
- K062046 — MODIFIED MERCI RETRIEVER, MODEL 90050
- K061059 — MODIFIED MERCI RETRIEVER, MODEL 90092
- K033736 — MERCI RETRIEVER, MODELS 90065, 90066
Data sourced from openFDA. This site is unofficial and independent of the FDA.