Inrad
Inrad holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2009.
Top product codes for Inrad
Recent clearances by Inrad
- K093399 — PRECISECORE 10 MM BIOPSY DEVICE- 14GA X 5 CM MODEL 670514, 671014, 670518 671018, 670520
- K093256 — SELECTCORE VARIABLE THROW BIOPSY DEVICE MODEL 991014, 991514, 991018, 991518, 992018
- K090611 — REVOLUTION FULL CORE BIOPSY
- K063238 — ULTRACLIP II WING AND ULTRACLIP II COIL
- K042341 — ULTRACLIP II US
- K041201 — ULTRACLIP II MR
- K000612 — ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE
- K993785 — ULTRACLIP TISSUE MARKER
- K981721 — C0-AXIAL INTRODUCER NEEDLE
- K981166 — ACCUCORE CORE BIOPSY NEEDLE CATALOG CODES:581014, 581614, 581618, 582018, 582518, 581620, 582020, 581214
- K980587 — IV DECANTER-FLEXIBLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.