510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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JODClass II

Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass

21 CFR 870.4270 / Cardiovascular
FDA source (opens on fda.gov)

JOD is the FDA product code for Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass, a class II device type, regulated under 21 CFR 870.4270. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JOD
Device name
Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
Regulation
21 CFR 870.4270
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
12
Ingested recalls
0

Clearances, product code JOD

By decision year
12 clearances under product code JOD with a decision year between 1978 and 2000, 1978 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JOD by decision year
YearClearances
19782
19811
19822
19831
19841
19861
19871
19881
19891
20001

Applicants with the most clearances

Product code JOD
Applicants holding the most 510(k) clearances under product code JOD
ApplicantClearances
Medical, Inc.4
Cobe Laboratories, Inc.2
Pall Biomedical Products Co.2
Gish Biomedical, Inc.1
Olson Medical Sales, Inc.1
Sterile Design, Inc.1
Texas Medical Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code