510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K192773Substantially Equivalent

Allive

NU Eyne Co., Ltd., Seoul, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K192773 is the FDA 510(k) clearance record for ALLIVE, a class II device, cleared for Nu Eyne Co., Ltd. on under FDA product code PCC (Stimulator, Nerve, Electrical, Transcutaneous, For Migraine). FDA's definition for product code PCC reads: "Used to apply an electrical current to a patient's cranium through electrodes placed on the skin". FDA records list 5 510(k) clearances for Nu Eyne Co., Ltd., from to . As of , FDA records show no recalls naming K192773.

Clearance record

Decision date
Received
(67 days to decision)
Product code
PCC Stimulator, Nerve, Electrical, Transcutaneous, For Migraine
Regulation
21 CFR 882.5891
Device class
Class II
Review panel
Neurology
Applicant
Nu Eyne Co., Ltd. #403, Seoul Biohub, 117-3 Hoegi-Ro, Dongdaemun-Gu, Seoul, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PCC

Trailing 12 months
1 clearance under product code PCC in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PCC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260