Medamicus, Inc.
Medamicus, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2004.
Top product codes for Medamicus, Inc.
Recent clearances by Medamicus, Inc.
- K040150 — MODIFICATION TO MEDAMICUS FLOWGUARD PEELABLE INTRODUCER
- K030905 — MEDAMICUS FLOWGUARD PEELABLE INTRODUCER
- K022689 — MODIFICATION TO MEDAMICUS AXIA RSN
- K021004 — VALVED PEELABLE INTRODUCER
- K020563 — MEDAMICUS AXIA RSN
- K013120 — PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18
- K011085 — GUIDEWIRE INTRODUCER SAFETY NEEDLE
- K000824 — PERCUTANEOUS INTRODUCER, MODEL 10383-XXX
- K994097 — MEDAMICUS EPIDURAL INTRODUCER
- K990705 — MEDAMICUS COAXIAL INTRODUCER KIT, 10330-XXX, BOSTON SCIENTIFIC COAXIAL DILATOR SET
- K965167 — PERCUTANEOUS VENOUS INTRODUCER 10264
- K971911 — LUMAX CYSTOMETRY ADMINISTRATION TUBE SET
- K953734 — LUMAX(MODIFICATION)
- K954093 — LUMAX (MODIFICATION)
- K951313 — MEDAMICUS PERCUTANEOUS INTRODUCER
- K944107 — VIP PLUS PERCUTANEOUS INTRODUCER
- K932323 — PERCUTANEOUS INTRODUCER
- K920580 — TRANSDUCER, PRESSURE, CATHETER TIP
- K924491 — INTRODUCER, PERCUTANEOUS -- MODIFICATION
- K893658 — PERCUTANEOUS INTRODUCER
Data sourced from openFDA. This site is unofficial and independent of the FDA.