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

Campylobacter Spp.

21 CFR 866.3110 / Microbiology
FDA source (opens on fda.gov)

LQP is the FDA product code for Campylobacter Spp., a class I device type, regulated under 21 CFR 866.3110. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LQP
Device name
Campylobacter Spp.
Regulation
21 CFR 866.3110
Device class
Class I
Review panel
Microbiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
12
Ingested recalls
1

Clearances, product code LQP

By decision year
12 clearances under product code LQP with a decision year between 1986 and 2021, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LQP by decision year
YearClearances
19862
19881
19981
20092
20182
20192
20212

Applicants with the most clearances

Product code LQP
Applicants holding the most 510(k) clearances under product code LQP
ApplicantClearances
Techlab, Inc.4
Meridian Bioscience Inc3
Alexon - Trend, Inc.1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Institute Virion, Ltd.1
Meridian Diagnostics, Inc.1
Ortho-Clinical Diagnostics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order