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

Transferrin, Rhodamine, Antigen, Antiserum, Control

21 CFR 866.5880 / Immunology
FDA source (opens on fda.gov)

DDD is the FDA product code for Transferrin, Rhodamine, Antigen, Antiserum, Control, a class II device type, regulated under 21 CFR 866.5880. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
DDD
Device name
Transferrin, Rhodamine, Antigen, Antiserum, Control
Regulation
21 CFR 866.5880
Device class
Class II
Review panel
Immunology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
1

Clearances, product code DDD

By decision year
1 clearance under product code DDD with a decision year between 1997 and 1997, 1997 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DDD by decision year
YearClearances
19971

Applicants with the most clearances

Product code DDD
Applicants holding the most 510(k) clearances under product code DDD
ApplicantClearances
OLYMPUS Corporation of the Americas1

Companies listing this code with FDA

Companies whose registered establishments list this code