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

Kappa, Fitc, Antigen, Antiserum, Control

21 CFR 866.5550 / Immunology
FDA source (opens on fda.gov)

DEO is the FDA product code for Kappa, Fitc, Antigen, Antiserum, Control, a class II device type, regulated under 21 CFR 866.5550. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DEO
Device name
Kappa, Fitc, Antigen, Antiserum, Control
Regulation
21 CFR 866.5550
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
2
Ingested recalls
0

Clearances, product code DEO

By decision year
2 clearances under product code DEO with a decision year between 1983 and 1983, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DEO by decision year
YearClearances
19832

Applicants with the most clearances

Product code DEO
Applicants holding the most 510(k) clearances under product code DEO
ApplicantClearances
Dako Corp.1
Gelco Diagnostics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code