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FDA 510(k)

VITALOGRAPH PFT PRINTER

K-Number: K823683 · 1983-01-21

ApplicantVitalograph , Ltd.
Decision Date1983-01-21
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITALOGRAPH PFT PRINTER is the device name listed in this FDA 510(k) record. The listed applicant is Vitalograph , Ltd.. It received FDA 510(k) clearance on 1983-01-21 under 510(k) number K823683. The device is classified under product code BTY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALOGRAPH PFT PRINTER?

VITALOGRAPH PFT PRINTER is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Vitalograph , Ltd.. The 510(k) number is K823683.

When did VITALOGRAPH PFT PRINTER receive FDA 510(k) clearance?

VITALOGRAPH PFT PRINTER received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823683.

Who is the listed applicant for VITALOGRAPH PFT PRINTER?

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

What is the FDA product code for VITALOGRAPH PFT PRINTER?

The FDA product code for VITALOGRAPH PFT PRINTER is BTY.

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 , Ltd. 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.

K253293VitaloJAK Clinic (Model 7100)K950854VITALOGRAPH 2110 SOFTWARE INTERFACEK925085ESCORT SPIROMETERK930085VITALOGRAPH DATA STORAGE SPIROMETERK912412VITALOGRAPH SPIROTRAC IIIK893665AEROSOL INHALATION MONITOR

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Related Devices (Code: BTY)

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.

K260242CPETWise PlatformMedibyt , Ltd.K242809Ascent Cardiorespiratory Diagnostic SoftwareMedical Graphics CorporationK223629SpiroSphere, SpiroSphereECG, CardioSphereEresearchtechnology GmbHK231561Pulmonary Function Tester, Model: A9Guangzhou Homesun Medical Technology Co., Ltd.K222982Virtus Metabolic MonitorVirtus Technology ApsK221030Model 9100 PFT/DICOVitalograph Ireland, 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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