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FDA 510(k)

WRIGHT VENTILOMETER VM-1

K-Number: K895953 · 1990-02-02

ApplicantClement Clarke, Inc.
Decision Date1990-02-02
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WRIGHT VENTILOMETER VM-1 is the device name listed in this FDA 510(k) record. The listed applicant is Clement Clarke, Inc.. It received FDA 510(k) clearance on 1990-02-02 under 510(k) number K895953. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIGHT VENTILOMETER VM-1?

WRIGHT VENTILOMETER VM-1 is a medical device that received FDA 510(k) clearance on 1990-02-02. The listed applicant is Clement Clarke, Inc.. The 510(k) number is K895953.

When did WRIGHT VENTILOMETER VM-1 receive FDA 510(k) clearance?

WRIGHT VENTILOMETER VM-1 received FDA 510(k) clearance on 1990-02-02, under 510(k) number K895953.

Who is the listed applicant for WRIGHT VENTILOMETER VM-1?

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

What is the FDA product code for WRIGHT VENTILOMETER VM-1?

The FDA product code for WRIGHT VENTILOMETER VM-1 is BZG.

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Other records listing Clement Clarke, 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.

K961512PERKINS HAND-HELD APPLANATION TONOMETERK952713MINI WRIGHT LR AFSK953965904 SLIT LAMPK932258OPTICOM M600K914126VMX MINI-LOG FLOWMETERK914896FRIEDMANN ANALYSER 3

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Related Devices (Code: BZG)

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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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