510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K172151Substantially Equivalent

Hysteroscopy System

Chongquin Jinshan Science & Technology (Group) Co., Ltd., Chongqing, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K172151 is the FDA 510(k) clearance record for Hysteroscopy System, a class II device, cleared for Chongquin Jinshan Science & Technology (Group) Co., Ltd. on under FDA product code HGH (Cannula, Suction, Uterine). FDA records list one 510(k) clearance for Chongquin Jinshan Science & Technology (Group) Co., Ltd. As of , FDA records show no recalls naming K172151.

Clearance record

Decision date
Received
(266 days to decision)
Product code
HGH Cannula, Suction, Uterine
Regulation
21 CFR 884.5070
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Chongquin Jinshan Science & Technology (Group) Co., Ltd. Yubei District #18 Ningshang Ave., Chongqing, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HGH

Trailing 12 months

FDA records hold no clearances under product code HGH in the trailing twelve months.

FDA records show no clearances under product code HGH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HGH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260