Mercury Rhinomanometer

No FDA recalls found in the data synced 6 Oct 2026.

510(k) Number

K902120 ↗

FDA Product Code

BXQ

Device Class

Class II

Regulation

21 CFR Part 868.1800

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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See all devices from Life-Tech Intl., Inc. →

• What is the primary clinical purpose of the Mercury Rhinomanometer?

  The Mercury Rhinomanometer is designed to assess nasal airway resistance and airflow characteristics. It functions as a rhinoanemometer to provide objective measurements of nasal decongestion for clinical evaluation.

• What is the regulatory status of this device?

  The Mercury Rhinomanometer has received FDA 510(k) clearance under the number K902120. It is classified under regulation number 868.1800 and is categorized under product code BXQ within the Anesthesiology medical specialty.

• Who is the manufacturer of the Mercury Rhinomanometer?

  The device is manufactured by Life-Tech Intl., Inc., based in Houston, Texas. The company submitted the device for regulatory review, which resulted in a determination of substantial equivalence.