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Avanos 181A440

by Avanos Medical, Inc.

Avanos 181A440 is a Class II device made by Avanos Medical, Inc., cleared under FDA 510(k) K000495 on 28 Mar 2000 and listed in FDA GUDID since 16 Oct 2020 (UDI-DI 00193493477470), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K000495

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00193493477470 UDI-DI Date16 Oct 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK000495 Date28 Mar 2000DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K000495 decided 28 Mar 2000 Active
  • FDA GUDID UDI-DI 00193493477470 listed 16 Oct 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K000495
  2. Listed FDA GUDID 00193493477470

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Avanos
Generic name
Peripheral anaesthesia single-administration set, non-medicated
Model / Ref / Catalog
181A440
Primary DI / UDI-DI
00193493477470
510(k) Number
FDA product code
BSP
GMDN term
Peripheral anaesthesia single-administration set, non-medicated
Device class
Class II
Regulation number
868.5150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BSP (NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)).

Other devices from Avanos Medical, Inc.

See all devices from Avanos Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)