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

Solution, Antimicrobial

21 CFR 866.1640 / Microbiology
FDA source (opens on fda.gov)

LOP is the FDA product code for Solution, Antimicrobial, a class II device type, regulated under 21 CFR 866.1640. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LOP
Device name
Solution, Antimicrobial
Regulation
21 CFR 866.1640
Device class
Class II
Review panel
Microbiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code LOP

By decision year
3 clearances under product code LOP with a decision year between 1981 and 1990, 1990 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LOP by decision year
YearClearances
19811
19902

Applicants with the most clearances

Product code LOP
Applicants holding the most 510(k) clearances under product code LOP
ApplicantClearances
The Upjohn Co.2
Cathra International, 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 LOP.