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FDA 510(k)

SPIROMETER, MODEL TS-500 PART #SLZ7534

K-Number: K855068 · 1986-02-05

ApplicantTeledyne Avionics Div. of Teledyne
Decision Date1986-02-05
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPIROMETER, MODEL TS-500 PART #SLZ7534 is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Avionics Div. of Teledyne. It received FDA 510(k) clearance on 1986-02-05 under 510(k) number K855068. 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 SPIROMETER, MODEL TS-500 PART #SLZ7534?

SPIROMETER, MODEL TS-500 PART #SLZ7534 is a medical device that received FDA 510(k) clearance on 1986-02-05. The listed applicant is Teledyne Avionics Div. of Teledyne. The 510(k) number is K855068.

When did SPIROMETER, MODEL TS-500 PART #SLZ7534 receive FDA 510(k) clearance?

SPIROMETER, MODEL TS-500 PART #SLZ7534 received FDA 510(k) clearance on 1986-02-05, under 510(k) number K855068.

Who is the listed applicant for SPIROMETER, MODEL TS-500 PART #SLZ7534?

The FDA 510(k) record lists Teledyne Avionics Div. of Teledyne as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPIROMETER, MODEL TS-500 PART #SLZ7534?

The FDA product code for SPIROMETER, MODEL TS-500 PART #SLZ7534 is BTY.

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Other records listing Teledyne Avionics Div. of Teledyne 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.

K860262TA-6C - PART NUMBER SLZ 7520K860522SPIROMETER, MODEL TS-1000, PART NO. SLZ7504K855069SPIROMETER TS-400 SLZ 7547K855070SPIROMETER MODEL TS-200 SLZ 7541K854043AUTOMATIC IMPEDANCE AUDIOMETER, TA-7BK851015TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER

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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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