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

Acid, Uric, Acid Reduction Of Ferric Ion

21 CFR 862.1775 / Clinical Chemistry
FDA source (opens on fda.gov)

LFQ is the FDA product code for Acid, Uric, Acid Reduction Of Ferric Ion, a class I device type, regulated under 21 CFR 862.1775. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LFQ
Device name
Acid, Uric, Acid Reduction Of Ferric Ion
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
1

Clearances, product code LFQ

By decision year
5 clearances under product code LFQ with a decision year between 1981 and 1986, 1981 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LFQ by decision year
YearClearances
19812
19841
19862

Applicants with the most clearances

Product code LFQ
Applicants holding the most 510(k) clearances under product code LFQ
ApplicantClearances
Anco Medical Reagents & Assoc.1
Livonia Diagnostics, Inc.1
Sandare Chemical Co., Inc.1
Sterling Diagnostics, Inc.1
Technostics Intl.1

Companies listing this code with FDA

Companies whose registered establishments list this code