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FDA 510(k)

MERCURY RHINOMANOMETER

K-Number: K902120 · 1990-08-06

ApplicantLife-Tech Intl., Inc.
Decision Date1990-08-06
Product CodeBXQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY RHINOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1990-08-06 under 510(k) number K902120. 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 MERCURY RHINOMANOMETER?

MERCURY RHINOMANOMETER is a medical device that received FDA 510(k) clearance on 1990-08-06. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K902120.

When did MERCURY RHINOMANOMETER receive FDA 510(k) clearance?

MERCURY RHINOMANOMETER received FDA 510(k) clearance on 1990-08-06, under 510(k) number K902120.

Who is the listed applicant for MERCURY RHINOMANOMETER?

The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERCURY RHINOMANOMETER?

The FDA product code for MERCURY RHINOMANOMETER is BXQ.

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Other records listing Life-Tech Intl., Inc. as applicant

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K001129PROLONG, MODELS PL50, PL100, PL150K955031MAXISTIMK954505EZ STIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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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

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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