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

Dna-Reagents, Mycoplasma Spp.

21 CFR 866.3375 / Microbiology
FDA source (opens on fda.gov)

LQG is the FDA product code for Dna-Reagents, Mycoplasma Spp., a class I device type, regulated under 21 CFR 866.3375. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
LQG
Device name
Dna-Reagents, Mycoplasma Spp.
Regulation
21 CFR 866.3375
Device class
Class I
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 LQG

By decision year
1 clearance under product code LQG with a decision year between 1986 and 1986, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LQG by decision year
YearClearances
19861

Applicants with the most clearances

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

Companies listing this code with FDA

Companies whose registered establishments list this code