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

Device, Discharge, Electrostatic (For Pain Relief)

21 CFR 890.5500 / Physical Medicine
FDA source (opens on fda.gov)

NHH is the FDA product code for Device, Discharge, Electrostatic (For Pain Relief), a class II device type, regulated under 21 CFR 890.5500. FDA's definition for this code reads: "An electrostatic discharge device which applies an electrostatic or coronal discharge to or near a person's skin for the symptomatic relief of pain". As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NHH
Device name
Device, Discharge, Electrostatic (For Pain Relief)
FDA definition
An electrostatic discharge device which applies an electrostatic or coronal discharge to or near a person's skin for the symptomatic relief of pain
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code NHH

By decision year
2 clearances under product code NHH with a decision year between 2001 and 2005, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NHH by decision year
YearClearances
20011
20051

Applicants with the most clearances

Product code NHH
Applicants holding the most 510(k) clearances under product code NHH
ApplicantClearances
Energex Systems, Inc.1
Orthosonix, 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 NHH.