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

Conductivity Rate, Urea Nitrogen

21 CFR 862.1770 / Clinical Chemistry
FDA source (opens on fda.gov)

LFP is the FDA product code for Conductivity Rate, Urea Nitrogen, a class II device type, regulated under 21 CFR 862.1770. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LFP
Device name
Conductivity Rate, Urea Nitrogen
Regulation
21 CFR 862.1770
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
6
Ingested recalls
0

Clearances, product code LFP

By decision year
6 clearances under product code LFP with a decision year between 1981 and 2000, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LFP by decision year
YearClearances
19811
19871
19931
19961
19991
20001

Applicants with the most clearances

Product code LFP
Applicants holding the most 510(k) clearances under product code LFP
ApplicantClearances
A-Kem, Inc.1
Amresco, Inc.1
Elan Holdings, Inc.1
Gambro Healthcare1
Sigma Chemical Co.1
Sigma Diagnostics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code