510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K030761Substantially Equivalent

Kaishou Vaginal Speculum

Jiangsu Kaishou Medical Apparatus Co., Ltd., Shanghai, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K030761 is the FDA 510(k) clearance record for KAISHOU VAGINAL SPECULUM, a class II device, cleared for Jiangsu Kaishou Medical Apparatus Co., Ltd. on under FDA product code HIB (Speculum, Vaginal, Nonmetal). FDA records list one 510(k) clearance for Jiangsu Kaishou Medical Apparatus Co., Ltd. As of , FDA records show no recalls naming K030761.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HIB Speculum, Vaginal, Nonmetal
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Jiangsu Kaishou Medical Apparatus Co., Ltd. 600 Liu Zhou Rd., Shanghai, CN
510(k) summary
Statement
Third party review
No

Clearances, product code HIB

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