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Oxygen Medicels, Citicels

by City Technology Limited

510(k) K041773

Oxygen Medicels, Citicels is a Class II device made by City Technology Limited, cleared under FDA 510(k) K041773 on 15 Jul 2004, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK041773 Date15 Jul 2004ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
CCL
Device class
Class II
Regulation
21 CFR Part 868.1720
Advisory committee
Anesthesiology
FDA decision
SESE Substantially Equivalent

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