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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Media, Reproductive
510(k) Number K240176
Device Name V-VITFREEZE and V-VITWARM
Applicant
Vitromed GmbH
Raiffeisenstr. 15a
Langenfeld,  DE 40764
Applicant Contact Holland Greg
Correspondent
Vitromed GmbH
Raiffeisenstr. 15a
Langenfeld,  DE 40764
Correspondent Contact Holland Greg
Regulation Number884.6180
Classification Product Code
MQL  
Date Received01/23/2024
Decision Date 09/13/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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