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Model 9160 VitaloQUB

by Vitalograph Ireland, Ltd. 510(k)

Active United States

510(k) K223818

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK223818 Date25 May 2023ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 11 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
JEH
Device Class
Class II
Regulation
21 CFR Part 868.1760
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

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