FDA 510(k)

SERV MEDICAL CDSS

K-Number: K241975 · 2025-03-17

Decision Date2025-03-17

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SERV MEDICAL CDSS is the device name listed in this FDA 510(k) record. The listed applicant is Serv Medical Pte., Ltd.. It received FDA 510(k) clearance on 2025-03-17 under 510(k) number K241975. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERV MEDICAL CDSS?

SERV MEDICAL CDSS is a medical device that received FDA 510(k) clearance on 2025-03-17. The listed applicant is Serv Medical Pte., Ltd.. The 510(k) number is K241975.

When did SERV MEDICAL CDSS receive FDA 510(k) clearance?

SERV MEDICAL CDSS received FDA 510(k) clearance on 2025-03-17, under 510(k) number K241975.

Who is the listed applicant for SERV MEDICAL CDSS?

The FDA 510(k) record lists Serv Medical Pte., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERV MEDICAL CDSS?

The FDA product code for SERV MEDICAL CDSS is LLZ.

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.