510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
QQCClass II

Brain Stimulation Programming Planning Software.

21 CFR 882.5855 / Neurology
FDA source (opens on fda.gov)

QQC is the FDA product code for Brain Stimulation Programming Planning Software., a class II device type, regulated under 21 CFR 882.5855. FDA's definition for this code reads: "The brain stimulation programming planning software is a prescription device intended to assist in planning stimulation programming for implanted brain stimulators". As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
QQC
Device name
Brain Stimulation Programming Planning Software.
FDA definition
The brain stimulation programming planning software is a prescription device intended to assist in planning stimulation programming for implanted brain stimulators.
Regulation
21 CFR 882.5855
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
3
Ingested recalls
0

Clearances, product code QQC

By decision year
3 clearances under product code QQC with a decision year between 2021 and 2025, 2021 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QQC by decision year
YearClearances
20211
20221
20251

Applicants with the most clearances

Product code QQC
Applicants holding the most 510(k) clearances under product code QQC
ApplicantClearances
Brainlab, Inc.1
Medtronic Neuromodulation1
Turing Medical Technologies, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code