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FDA 510(k)

Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)

K-Number: K261582 · 2026-08-28

Decision Date2026-08-28
Product CodeNUV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02) is the device name listed in this FDA 510(k) record. The listed applicant is Zhengzhou PZ Laser Slim Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-08-28 under 510(k) number K261582. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)?

Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02) is a medical device that received FDA 510(k) clearance on 2026-08-28. The listed applicant is Zhengzhou PZ Laser Slim Technology Co., Ltd.. The 510(k) number is K261582.

When did Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02) receive FDA 510(k) clearance?

Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02) received FDA 510(k) clearance on 2026-08-28, under 510(k) number K261582.

Who is the listed applicant for Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)?

The FDA 510(k) record lists Zhengzhou PZ Laser Slim Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)?

The FDA product code for Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02) is NUV.

Other records listing Zhengzhou PZ Laser Slim Technology Co., Ltd. as applicant

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.

View all 8 devices →

Related Devices (Code: NUV)

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.

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.