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FDA 510(k)

VITALOGRAPH MODEL 2120

K-Number: K946075 · 1995-08-04

ApplicantVitalograph, Inc.
Decision Date1995-08-04
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITALOGRAPH MODEL 2120 is the device name listed in this FDA 510(k) record. The listed applicant is Vitalograph, Inc.. It received FDA 510(k) clearance on 1995-08-04 under 510(k) number K946075. 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 VITALOGRAPH MODEL 2120?

VITALOGRAPH MODEL 2120 is a medical device that received FDA 510(k) clearance on 1995-08-04. The listed applicant is Vitalograph, Inc.. The 510(k) number is K946075.

When did VITALOGRAPH MODEL 2120 receive FDA 510(k) clearance?

VITALOGRAPH MODEL 2120 received FDA 510(k) clearance on 1995-08-04, under 510(k) number K946075.

Who is the listed applicant for VITALOGRAPH MODEL 2120?

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

What is the FDA product code for VITALOGRAPH MODEL 2120?

The FDA product code for VITALOGRAPH MODEL 2120 is BZG.

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 Vitalograph, 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.

K000599VITALOGRAPH BASE STATIONK991412VITALOGRAPH MICROK943678ELECTRONIC FLOW METERK942779DISPOSABLE BACTERIOLOGICAL FILTER

Related Devices (Code: BZG)

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.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

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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