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FDA 510(k)

PTT-200 TELEPHONIC PULMONARY TRANSMITT

K-Number: K812849 · 1981-12-03

ApplicantPharmaquest Corp.
Decision Date1981-12-03
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PTT-200 TELEPHONIC PULMONARY TRANSMITT is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaquest Corp.. It received FDA 510(k) clearance on 1981-12-03 under 510(k) number K812849. 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 PTT-200 TELEPHONIC PULMONARY TRANSMITT?

PTT-200 TELEPHONIC PULMONARY TRANSMITT is a medical device that received FDA 510(k) clearance on 1981-12-03. The listed applicant is Pharmaquest Corp.. The 510(k) number is K812849.

When did PTT-200 TELEPHONIC PULMONARY TRANSMITT receive FDA 510(k) clearance?

PTT-200 TELEPHONIC PULMONARY TRANSMITT received FDA 510(k) clearance on 1981-12-03, under 510(k) number K812849.

Who is the listed applicant for PTT-200 TELEPHONIC PULMONARY TRANSMITT?

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

What is the FDA product code for PTT-200 TELEPHONIC PULMONARY TRANSMITT?

The FDA product code for PTT-200 TELEPHONIC PULMONARY TRANSMITT is BTY.

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Other records listing Pharmaquest Corp. 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.

K945519FACE (FLUOROPHORE-ASSISTED-CARBOHYDRATE-ELECTROPHORESIS) URINARY CARBOHYDRATE ANALYSIS SYSTEMK833880TELEPHONIC RECEIVER R-10 EEGK833236TELEPHONE TRANSMITTER T-10 EEGK830705MINI LANCET-BLOOD LANCETK822976HYPOCOUNT AK822486HOME BLOOD GLUCOSE 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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