FDA 510(k) clearance · back to tracker
Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)
Zhengzhou PZ Laser Slim Technology Co., Ltd. cleared K261582 on 2026-08-28, decision: substantially equivalent
K-number
K261582
Sponsor
Zhengzhou PZ Laser Slim Technology Co., Ltd.
Device
Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)
Class
Class II
Decision
Substantially Equivalent
Decision date
2026-08-28
Product code
NUV
Advisory committee
General, Plastic Surgery
Medical specialty
General, Plastic Surgery
Regulation number
878.4810
Official FDA record
Open K261582on accessdata.fda.gov →
FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.
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Raw record →
Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.
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Try the sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.