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FDA 510(k)

COMPAS

K-Number: K021200 · 2002-10-18

ApplicantMorgan Scientific, Inc.
Decision Date2002-10-18
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPAS is the device name listed in this FDA 510(k) record. The listed applicant is Morgan Scientific, Inc.. It received FDA 510(k) clearance on 2002-10-18 under 510(k) number K021200. 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 COMPAS?

COMPAS is a medical device that received FDA 510(k) clearance on 2002-10-18. The listed applicant is Morgan Scientific, Inc.. The 510(k) number is K021200.

When did COMPAS receive FDA 510(k) clearance?

COMPAS received FDA 510(k) clearance on 2002-10-18, under 510(k) number K021200.

Who is the listed applicant for COMPAS?

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

What is the FDA product code for COMPAS?

The FDA product code for COMPAS is BZG.

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Other records listing Morgan Scientific, 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.

K213872ComPAS2K190568ComPAS2 (Computerized Pulmonary Analysis System)K042595SPIRO'AIRK022636BODY BOX 5500K013752COMPAS AS (COMPUTERIZED PULMONARY ANALYSIS SYSTEM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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