Single Use Guide Sheath Kit K-401, K-402, & Single Use Guiding Device CC-220DR

by Olympus Medical Systems Corp. 510(k)

Active United States

510(k) K192164

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK192164	Date6 Mar 2020Cleared	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Withdrawn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: K192164
FDA Product Code: EOQ

Device Class: Class II
Regulation: 21 CFR Part 874.4680
Advisory Committee: Ear, Nose, Throat
FDA Decision: SESE Substantially Equivalent

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