Product code JOD— Cardiovascular
INTERFACE CARDIOTOMY BLOOD FILTER #51
- Classification name
- Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
- Device class
- Class 2
- Regulation
- 21 CFR 870.4270
- Advisory panel
- Cardiovascular
- Total cleared
- 12
- First cleared
- Most recent
Market context for product code JOD
FDA has cleared devices under product code JOD between 1978 and 2000, filed by 7 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2000
- 1989
- 1988
- 1987
- 1986
- 1984
- 1983
- 1982
- 1981
- 1978
Top applicants under product code JOD
Recent clearances under product code JOD
- K993060 — GAS FILTER
- K890504 — CARDIOTOMY/AUTOTRANSFUSION/PLEURAL DRAINAGE VENOUS
- K875095 — PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE
- K874405 — PALL STAT PRIME(TM) BLOOD FILTER FOR EXTRA. USE
- K855067 — SWANK CARDIOTOMY SUCTION LINE BLOOD FILTER CA100
- K841958 — CARDIO METRICS CARDIOTOMY RESERVOIR
- K830634 — CARDIOTOMY FILTER
- K823259 — INTERFACE CARDIOTOMY BLOOD FILTER #50
- K823260 — INTERFACE CARDIOTOMY BLOOD FILTER #51
- K812243 — INTERFACE CARDIOTOMY BLOOD FILTER #51
- K781383 — INTERFACE CARDIOTOMY BLOOD FILTER
- K780653 — EXTRACORPEAL CARDIOTOMY BLOOD FILTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.