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

Solution, Cold Sterilizing

21 CFR 880.6885 / General Hospital
FDA source (opens on fda.gov)

LFE is the FDA product code for Solution, Cold Sterilizing, a class II device type, regulated under 21 CFR 880.6885. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LFE
Device name
Solution, Cold Sterilizing
Regulation
21 CFR 880.6885
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code LFE

By decision year
1 clearance under product code LFE with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LFE by decision year
YearClearances
19831

Applicants with the most clearances

Product code LFE
Applicants holding the most 510(k) clearances under product code LFE
ApplicantClearances
North Pacific Dental, 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 LFE.