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Lung Diffusion Gas Mixtures

by Norco, Inc.

510(k) K911471

Lung Diffusion Gas Mixtures is a Class I device made by Norco, Inc., cleared under FDA 510(k) K911471 on 18 Jun 1991, active as of 11 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 11 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 11 Oct 2026.

Regulatory status

as of registry sync 11 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK911471 Date18 Jun 1991ClearedStatusActive

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  • Withdrawn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
BXK
Device class
Class I
Regulation
21 CFR Part 868.6400
Advisory committee
Anesthesiology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code BXK (Gas, Calibration (Specified Concentration)).

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