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FDA 510(k)

SPIROMETER, MODEL TS-1000, PART NO. SLZ7504

K-Number: K860522 · 1986-03-03

ApplicantTeledyne Avionics Div. of Teledyne
Decision Date1986-03-03
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPIROMETER, MODEL TS-1000, PART NO. SLZ7504 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 1986-03-03 under 510(k) number K860522. 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 SPIROMETER, MODEL TS-1000, PART NO. SLZ7504?

SPIROMETER, MODEL TS-1000, PART NO. SLZ7504 is a medical device that received FDA 510(k) clearance on 1986-03-03. The listed applicant is Teledyne Avionics Div. of Teledyne. The 510(k) number is K860522.

When did SPIROMETER, MODEL TS-1000, PART NO. SLZ7504 receive FDA 510(k) clearance?

SPIROMETER, MODEL TS-1000, PART NO. SLZ7504 received FDA 510(k) clearance on 1986-03-03, under 510(k) number K860522.

Who is the listed applicant for SPIROMETER, MODEL TS-1000, PART NO. SLZ7504?

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-1000, PART NO. SLZ7504?

The FDA product code for SPIROMETER, MODEL TS-1000, PART NO. SLZ7504 is BZG.

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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 7520K855068SPIROMETER, MODEL TS-500 PART #SLZ7534K855069SPIROMETER TS-400 SLZ 7547K855070SPIROMETER MODEL TS-200 SLZ 7541K854043AUTOMATIC IMPEDANCE AUDIOMETER, TA-7BK851015TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER

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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

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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