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FDA 510(k)

PB900 PB910 DIAGNOSTIC SPIROMETER

K-Number: K852092 · 1985-07-30

ApplicantPuritan Bennett Corp.
Decision Date1985-07-30
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PB900 PB910 DIAGNOSTIC SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1985-07-30 under 510(k) number K852092. 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 PB900 PB910 DIAGNOSTIC SPIROMETER?

PB900 PB910 DIAGNOSTIC SPIROMETER is a medical device that received FDA 510(k) clearance on 1985-07-30. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K852092.

When did PB900 PB910 DIAGNOSTIC SPIROMETER receive FDA 510(k) clearance?

PB900 PB910 DIAGNOSTIC SPIROMETER received FDA 510(k) clearance on 1985-07-30, under 510(k) number K852092.

Who is the listed applicant for PB900 PB910 DIAGNOSTIC SPIROMETER?

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

What is the FDA product code for PB900 PB910 DIAGNOSTIC SPIROMETER?

The FDA product code for PB900 PB910 DIAGNOSTIC SPIROMETER is BZG.

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Other records listing Puritan Bennett Corp. as applicant

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K063650VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840K053388MODEL 840 VENTILATOR WITH PROPORTIONAL ASSIST VENTILATION PLUS SOFTWARE OPTIONK023225PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWAREK022103PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEMK001646PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTIONK002001BREEZE SLEEPGEAR WITH DREAMSEAL

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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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