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FDA 510(k)

RHINOMANOMETER A440 DIGITAL

K-Number: K844230 · 1984-11-27

ApplicantCenter Laboratories, Inc.
Decision Date1984-11-27
Product CodeBXQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RHINOMANOMETER A440 DIGITAL is the device name listed in this FDA 510(k) record. The listed applicant is Center Laboratories, Inc.. It received FDA 510(k) clearance on 1984-11-27 under 510(k) number K844230. 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 RHINOMANOMETER A440 DIGITAL?

RHINOMANOMETER A440 DIGITAL is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Center Laboratories, Inc.. The 510(k) number is K844230.

When did RHINOMANOMETER A440 DIGITAL receive FDA 510(k) clearance?

RHINOMANOMETER A440 DIGITAL received FDA 510(k) clearance on 1984-11-27, under 510(k) number K844230.

Who is the listed applicant for RHINOMANOMETER A440 DIGITAL?

The FDA 510(k) record lists Center Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RHINOMANOMETER A440 DIGITAL?

The FDA product code for RHINOMANOMETER A440 DIGITAL 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.

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Other records listing Center Laboratories, Inc. 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.

K954277ASTECH PEAK FLOW METER

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 SolutionsK022311RHINOSTREAM RHINOMANOMETER MODULERhino Metrics A/SK011329ECCOVISION 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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