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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 the device name listed in this FDA 510(k) record. The listed applicant is Curative Sound Therapeutics. It received FDA 510(k) clearance on 2025-07-02 under 510(k) 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. The listed applicant is Curative Sound Therapeutics. The 510(k) number is K250779.

When did CS-Pro MED receive FDA 510(k) clearance?

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

Who is the listed applicant for CS-Pro MED?

The FDA 510(k) record lists Curative Sound Therapeutics as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: PZL)

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.

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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.

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