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FDA 510(k)

MULTISPIRO

K-Number: K895375 · 1989-11-27

ApplicantMedical Equipment Designs, Inc.
Decision Date1989-11-27
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MULTISPIRO is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Designs, Inc.. It received FDA 510(k) clearance on 1989-11-27 under 510(k) number K895375. 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 MULTISPIRO?

MULTISPIRO is a medical device that received FDA 510(k) clearance on 1989-11-27. The listed applicant is Medical Equipment Designs, Inc.. The 510(k) number is K895375.

When did MULTISPIRO receive FDA 510(k) clearance?

MULTISPIRO received FDA 510(k) clearance on 1989-11-27, under 510(k) number K895375.

Who is the listed applicant for MULTISPIRO?

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

What is the FDA product code for MULTISPIRO?

The FDA product code for MULTISPIRO is BZG.

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Other records listing Medical Equipment Designs, 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.

K911308CARDIOTRACE-I TRANSTELEPHONIC ECG RECEIV CONSOLEK894152MEDITHERMK851277MICROSPIRO-SDSK840929FRC 85 SERIES SPIROMETERK840908CHESTAC-25F SPIROMETERK821082TRIAL LENS SET

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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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