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

Antigens, All Groups, Shigella Spp.

21 CFR 866.3660 / Microbiology
FDA source (opens on fda.gov)

LIA is the FDA product code for Antigens, All Groups, Shigella Spp., a class II device type, regulated under 21 CFR 866.3660. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
LIA
Device name
Antigens, All Groups, Shigella Spp.
Regulation
21 CFR 866.3660
Device class
Class II
Review panel
Microbiology
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
1

Clearances, product code LIA

By decision year
1 clearance under product code LIA with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LIA by decision year
YearClearances
19811

Applicants with the most clearances

Product code LIA
Applicants holding the most 510(k) clearances under product code LIA
ApplicantClearances
Lab Ability, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LIA.