Avanticare, Model SA4021

by Lerado China Limited 510(k)

Active United States

510(k) K060068

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK060068	Date8 Mar 2006Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K060068
FDA Product Code: INI

Device Class: Class II
Regulation: 21 CFR Part 890.3800
Advisory Committee: Physical Medicine
FDA Decision: SESE Substantially Equivalent

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