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FDA 510(k)

COLLINS PNEUMOTACH PFT SYSTEM

K-Number: K861227 · 1986-06-05

ApplicantWarren E. Collins, Inc.
Decision Date1986-06-05
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COLLINS PNEUMOTACH PFT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Warren E. Collins, Inc.. It received FDA 510(k) clearance on 1986-06-05 under 510(k) number K861227. 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 COLLINS PNEUMOTACH PFT SYSTEM?

COLLINS PNEUMOTACH PFT SYSTEM is a medical device that received FDA 510(k) clearance on 1986-06-05. The listed applicant is Warren E. Collins, Inc.. The 510(k) number is K861227.

When did COLLINS PNEUMOTACH PFT SYSTEM receive FDA 510(k) clearance?

COLLINS PNEUMOTACH PFT SYSTEM received FDA 510(k) clearance on 1986-06-05, under 510(k) number K861227.

Who is the listed applicant for COLLINS PNEUMOTACH PFT SYSTEM?

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

What is the FDA product code for COLLINS PNEUMOTACH PFT SYSTEM?

The FDA product code for COLLINS PNEUMOTACH PFT SYSTEM is BZG.

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Other records listing Warren E. Collins, 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.

K925459GS-MODULAR (GOLD STANDARD - MODULAR)K912946COLLINS DIGITAL PULMONARY MANOMETERK871151THE SPIRA ELEKTRO 2K852102COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEMK831780METABOLIC EXERCISE TESTING SYSTEMK831778RS-RESIDUAL VOLUME SYSTEM

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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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