Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM

K-Number: K920111 · 1992-10-26

ApplicantSensor Medics Corp.
Decision Date1992-10-26
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sensor Medics Corp.. It received FDA 510(k) clearance on 1992-10-26 under 510(k) number K920111. 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 SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM?

SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 1992-10-26. The listed applicant is Sensor Medics Corp.. The 510(k) number is K920111.

When did SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM receive FDA 510(k) clearance?

SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM received FDA 510(k) clearance on 1992-10-26, under 510(k) number K920111.

Who is the listed applicant for SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM?

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

What is the FDA product code for SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM?

The FDA product code for SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sensor Medics Corp. 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.

K032516HIOX80 AEROSOL ADAPTERK031745INFANT FLOW PLUS INFANT CPAP SYSTEM WITH SIPAP FUNCTIONK031883LYRA NASAL MASKK030943MODIFICATION TO HIOXK022192PEGASUS NASAL CPAP SYSTEMK020665HI-OX

View all 26 devices →

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.

↑