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FDA 510(k)

MODEL 2800 PFT FILTER

K-Number: K051712 · 2005-09-01

ApplicantAir Safety, Ltd.
Decision Date2005-09-01
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 2800 PFT FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Air Safety, Ltd.. It received FDA 510(k) clearance on 2005-09-01 under 510(k) number K051712. 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 MODEL 2800 PFT FILTER?

MODEL 2800 PFT FILTER is a medical device that received FDA 510(k) clearance on 2005-09-01. The listed applicant is Air Safety, Ltd.. The 510(k) number is K051712.

When did MODEL 2800 PFT FILTER receive FDA 510(k) clearance?

MODEL 2800 PFT FILTER received FDA 510(k) clearance on 2005-09-01, under 510(k) number K051712.

Who is the listed applicant for MODEL 2800 PFT FILTER?

The FDA 510(k) record lists Air Safety, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 2800 PFT FILTER?

The FDA product code for MODEL 2800 PFT FILTER is BZG.

Related Clinical Trials

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.

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Other records listing Air Safety, Ltd. 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.

K050953AIR SAFETY MODEL 3000/06 FILTER HEPA REUSABLEK040712AIR SAFETY HEPA, MODEL 3500K033008AIR SAFETY HEPA AND NON-HEPA FILTERS

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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