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

Whole Blood Plasma, Antigen, Antiserum, Control

21 CFR 866.5700 / Immunology
FDA source (opens on fda.gov)

DGQ is the FDA product code for Whole Blood Plasma, Antigen, Antiserum, Control, a class I device type, regulated under 21 CFR 866.5700. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DGQ
Device name
Whole Blood Plasma, Antigen, Antiserum, Control
Regulation
21 CFR 866.5700
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
1
Ingested recalls
0

Clearances, product code DGQ

By decision year
1 clearance under product code DGQ with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DGQ by decision year
YearClearances
19791

Applicants with the most clearances

Product code DGQ
Applicants holding the most 510(k) clearances under product code DGQ
ApplicantClearances
Diagnostica, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code