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

Electromagnetic Stimulator, Pain Relief

21 CFR 882.5890 / Neurology
FDA source (opens on fda.gov)

QPL is the FDA product code for Electromagnetic Stimulator, Pain Relief, a class II device type, regulated under 21 CFR 882.5890. FDA's definition for this code reads: "Intended to apply a magnetic-field induced electrical current to treat pain". As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
QPL
Device name
Electromagnetic Stimulator, Pain Relief
FDA definition
Intended to apply a magnetic-field induced electrical current to treat pain.
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
6
Ingested recalls
0

Clearances, product code QPL

By decision year
6 clearances under product code QPL with a decision year between 2021 and 2025, 2025 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code QPL by decision year
YearClearances
20211
20231
20241
20253

Applicants with the most clearances

Product code QPL
Applicants holding the most 510(k) clearances under product code QPL
ApplicantClearances
Neuralace Medical2
BTL Industries, Inc1
Fotona d.o.o.1
Magstim Inc.1
Tonica Elektronik a/S1

Companies listing this code with FDA

Companies whose registered establishments list this code