Disposable Trocars

FDA 510(k) K233263 · Hangzhou Kangji Medical Instrument Co., Ltd.

Substantially Equivalent

510(k) numberK233263

Submission

Device name
Disposable Trocars
Applicant
Hangzhou Kangji Medical Instrument Co., Ltd.
Hangzhou, CN
Received
September 29, 2023
Decision date
April 9, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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More from TroCare, LLC

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K250643Disposable Polymer Ligation ClipsFZP · Traditional 11/20/2025SE
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Questions and answers

When was Disposable Trocars cleared by the FDA?

Disposable Trocars (K233263) received a 510(k) decision of Substantially Equivalent on April 9, 2024, 193 days after the submission was received.

What is the product code of K233263?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.