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

Electrode Measurement, Drain Effluent Ph

21 CFR 862.1120 / Clinical Chemistry
FDA source (opens on fda.gov)

SFO is the FDA product code for Electrode Measurement, Drain Effluent Ph, a class II device type, regulated under 21 CFR 862.1120. FDA's definition for this code reads: "Measurement of drain effluent pH". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
SFO
Device name
Electrode Measurement, Drain Effluent Ph
FDA definition
Measurement of drain effluent pH
Regulation
21 CFR 862.1120
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
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code SFO

By decision year
1 clearance under product code SFO with a decision year between 2025 and 2025, 2025 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code SFO by decision year
YearClearances
20251

Applicants with the most clearances

Product code SFO
Applicants holding the most 510(k) clearances under product code SFO
ApplicantClearances
Nerv Technology Inc. (D.B.A.) Fluidai Medical1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code SFO.