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

Igg, Peroxidase, Antigen, Antiserum, Control

21 CFR 866.5510 / Immunology
FDA source (opens on fda.gov)

DAA is the FDA product code for Igg, Peroxidase, Antigen, Antiserum, Control, a class II device type, regulated under 21 CFR 866.5510. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DAA
Device name
Igg, Peroxidase, Antigen, Antiserum, Control
Regulation
21 CFR 866.5510
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
5
Ingested recalls
0

Clearances, product code DAA

By decision year
5 clearances under product code DAA with a decision year between 1979 and 1983, 1983 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code DAA by decision year
YearClearances
19791
19821
19833

Applicants with the most clearances

Product code DAA
Applicants holding the most 510(k) clearances under product code DAA
ApplicantClearances
Clinical Sciences, Inc.3
Breit Laboratories, Inc.1
Diagnostic Reagent Tech.1

Companies listing this code with FDA

Companies whose registered establishments list this code