Mercury Rhinomanometer
FDA 510(k) K902120 · Life-Tech Intl., Inc.
510(k) numberK902120
Submission
- Device name
- Mercury Rhinomanometer
- Applicant
- Life-Tech Intl., Inc.
Houston, TX, US - Received
- May 11, 1990
- Decision date
- August 6, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BXQ – Rhinoanemometer (Measurement Of Nasal Decongestion)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.1800
- Specialty
- Anesthesiology
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Questions and answers
When was Mercury Rhinomanometer cleared by the FDA?
Mercury Rhinomanometer (K902120) received a 510(k) decision of Substantially Equivalent on August 6, 1990, 87 days after the submission was received.
What is the product code of K902120?
The FDA product code is BXQ – Rhinoanemometer (Measurement Of Nasal Decongestion), a Class II (moderate risk) device regulated under 21 CFR 868.1800.