510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K250033Substantially Equivalent

Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)

Guangzhou Pinzhi Medical Technology Co., Ltd, Guangzhou, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K250033 is the FDA 510(k) clearance record for Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E), a class II device, cleared for Guangzhou Pinzhi Medical Technology Co., Ltd. on under FDA product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter). FDA's definition for product code NUH reads: "TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES". FDA records list one 510(k) clearance for Guangzhou Pinzhi Medical Technology Co., Ltd. As of , FDA records show no recalls naming K250033.

Clearance record

Decision date
Received
(90 days to decision)
Product code
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
Guangzhou Pinzhi Medical Technology Co., Ltd. Rm. 501/601-1, Unit 01, Bldg. 2, Number 44,, Guangzhou, CN
510(k) summary
Statement
Third party review
No

Clearances, product code NUH

Trailing 12 months
10 clearances under product code NUH in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code NUH, trailing twelve months
MonthClearances
November 20253
December 20253
January 20260
February 20260
March 20261
April 20260
May 20260
June 20262
July 20260
August 20260
September 20261
October 20260