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FDA 510(k)

CS-Pro MED

K-Number: K250779 · 2025-07-02

ApplicantCurative Sound Therapeutics
Decision Date2025-07-02
Product CodePZL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CS-Pro MED is a medical device manufactured by Curative Sound Therapeutics. It received FDA 510(k) clearance on 2025-07-02 under approval number K250779. The device is classified under product code PZL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CS-Pro MED?

CS-Pro MED is a medical device that received FDA 510(k) clearance on 2025-07-02. It is manufactured by Curative Sound Therapeutics. The 510(k) number is K250779.

When was CS-Pro MED approved by the FDA?

CS-Pro MED received FDA 510(k) clearance on 2025-07-02, under approval number K250779.

What company makes CS-Pro MED?

CS-Pro MED is manufactured by Curative Sound Therapeutics.

What is the FDA product code for CS-Pro MED?

The FDA product code for CS-Pro MED is PZL.

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Official Source

View on FDA Database →

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

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