A1 ACOUSTIC RHINOMETER
K-Number: K972140 · 1998-09-30
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Device Summary
Frequently Asked Questions
What is the A1 ACOUSTIC RHINOMETER?
A1 ACOUSTIC RHINOMETER is a medical device that received FDA 510(k) clearance on 1998-09-30. The listed applicant is G.M. Instruments , Ltd.. The 510(k) number is K972140.
When did A1 ACOUSTIC RHINOMETER receive FDA 510(k) clearance?
A1 ACOUSTIC RHINOMETER received FDA 510(k) clearance on 1998-09-30, under 510(k) number K972140.
Who is the listed applicant for A1 ACOUSTIC RHINOMETER?
The FDA 510(k) record lists G.M. Instruments , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A1 ACOUSTIC RHINOMETER?
The FDA product code for A1 ACOUSTIC RHINOMETER is BXQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BXQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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