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

Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch

21 CFR 882.5894 / Neurology
FDA source (opens on fda.gov)

OSG is the FDA product code for Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch, a class II device type, regulated under 21 CFR 882.5894. FDA's definition for this code reads: "Relief / Reduction of Mosquito Bite Itch". As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
OSG
Device name
Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch
FDA definition
Relief / Reduction of Mosquito Bite Itch
Regulation
21 CFR 882.5894
Device class
Class II
Review panel
Neurology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code OSG

By decision year
2 clearances under product code OSG with a decision year between 2014 and 2014, 2014 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code OSG by decision year
YearClearances
20142

Applicants with the most clearances

Product code OSG
Applicants holding the most 510(k) clearances under product code OSG
ApplicantClearances
Ecobrands, Ltd.1
Tecnimed S.r.l.1

Companies listing this code with FDA

Companies whose registered establishments list this code