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FDA 510(k)

SCHILLER MODEL SP-200 SPIROVIT(TM)

K-Number: K896121 · 1990-01-09

ApplicantSchiller America, Inc.
Decision Date1990-01-09
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SCHILLER MODEL SP-200 SPIROVIT(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Schiller America, Inc.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K896121. 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 SCHILLER MODEL SP-200 SPIROVIT(TM)?

SCHILLER MODEL SP-200 SPIROVIT(TM) is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is Schiller America, Inc.. The 510(k) number is K896121.

When did SCHILLER MODEL SP-200 SPIROVIT(TM) receive FDA 510(k) clearance?

SCHILLER MODEL SP-200 SPIROVIT(TM) received FDA 510(k) clearance on 1990-01-09, under 510(k) number K896121.

Who is the listed applicant for SCHILLER MODEL SP-200 SPIROVIT(TM)?

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

What is the FDA product code for SCHILLER MODEL SP-200 SPIROVIT(TM)?

The FDA product code for SCHILLER MODEL SP-200 SPIROVIT(TM) is BZG.

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Other records listing Schiller America, 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.

K973735MICROVIT MT-100K973751MT-200K970879CARDIOVIT CS-200K953396CARDIOVIT AT-1C, AT-2CK954066MINISCOPE MS-3K941462CARDIOVIT AT-5C

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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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