FDA 510(k) Application Details - K221178

Device Classification Name Needle, Hypodermic, Single Lumen

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510(K) Number K221178
Device Name Needle, Hypodermic, Single Lumen
Applicant Ningbo Medsun Medical Co., Ltd.
No.55 Jinxi Road, Zhenhai
Ningbo 315221 CN
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Contact Liu Ping
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Regulation Number 880.5570

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Classification Product Code FMI
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Date Received 04/25/2022
Decision Date 11/17/2022
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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