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

Lactoferrin, Antigen, Antiserum, Control

21 CFR 866.5570 / Immunology
FDA source (opens on fda.gov)

DEG is the FDA product code for Lactoferrin, Antigen, Antiserum, Control, a class I device type, regulated under 21 CFR 866.5570. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
DEG
Device name
Lactoferrin, Antigen, Antiserum, Control
Regulation
21 CFR 866.5570
Device class
Class I
Review panel
Immunology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
8
Ingested recalls
1

Clearances, product code DEG

By decision year
8 clearances under product code DEG with a decision year between 1985 and 2007, 1993 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DEG by decision year
YearClearances
19851
19932
19951
20011
20031
20041
20071

Applicants with the most clearances

Product code DEG
Applicants holding the most 510(k) clearances under product code DEG
ApplicantClearances
Techlab, Inc.4
Touch Scientific, Inc.2
Mackeen Consultants, Ltd.1
Techlab Inc., Corporate Research Center1

Companies listing this code with FDA

Companies whose registered establishments list this code