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FDA 510(k)

RHINOSTREAM RHINOMANOMETER MODULE

K-Number: K022311 · 2002-10-04

ApplicantRhino Metrics A/S
Decision Date2002-10-04
Product CodeBXQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RHINOSTREAM RHINOMANOMETER MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Rhino Metrics A/S. It received FDA 510(k) clearance on 2002-10-04 under 510(k) number K022311. The device is classified under product code BXQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHINOSTREAM RHINOMANOMETER MODULE?

RHINOSTREAM RHINOMANOMETER MODULE is a medical device that received FDA 510(k) clearance on 2002-10-04. The listed applicant is Rhino Metrics A/S. The 510(k) number is K022311.

When did RHINOSTREAM RHINOMANOMETER MODULE receive FDA 510(k) clearance?

RHINOSTREAM RHINOMANOMETER MODULE received FDA 510(k) clearance on 2002-10-04, under 510(k) number K022311.

Who is the listed applicant for RHINOSTREAM RHINOMANOMETER MODULE?

The FDA 510(k) record lists Rhino Metrics A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RHINOSTREAM RHINOMANOMETER MODULE?

The FDA product code for RHINOSTREAM RHINOMANOMETER MODULE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Rhino Metrics A/S as applicant

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.

K000406RHINOSCAN MODEL SRE2000/ SRE2100 WITH ACOUSTIC RHINOMETRY MODULE

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.

K221892VISIONAIRPacificmd Biotech, LLCK170071SGS ECCOVISIONTM Pharyngometer, SGS ECCOVISIONTM Rhinometer, SGS ECCOVISIONTM Rhino/PharyngometerSleep Group SolutionsK011329ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETERE. Benson Hood Lab, Inc.K000406RHINOSCAN MODEL SRE2000/ SRE2100 WITH ACOUSTIC RHINOMETRY MODULERhino Metrics A/SK972140A1 ACOUSTIC RHINOMETERG.M. Instruments , Ltd.K921452ACOUSTIC RHINOMETERHood Laboratories

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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