K-number	K234124
Device name	Single Use Hemoclips
Applicant	Promisemed Hangzhou Meditech Co., Ltd.
Product code	PKL
Device class	Class II
Decision date	Jul 12, 2024
Decision	Substantially Equivalent
Regulation	876.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Single Use Hemoclips

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