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 2600 PEDIATRIC PULMOONARY CART

K-Number: K915833 · 1992-12-02

ApplicantSensor Medics Corp.
Decision Date1992-12-02
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART 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 1992-12-02 under 510(k) number K915833. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART?

SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART is a medical device that received FDA 510(k) clearance on 1992-12-02. The listed applicant is Sensor Medics Corp.. The 510(k) number is K915833.

When did SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART receive FDA 510(k) clearance?

SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART received FDA 510(k) clearance on 1992-12-02, under 510(k) number K915833.

Who is the listed applicant for SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART?

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 2600 PEDIATRIC PULMOONARY CART?

The FDA product code for SENSORMEDICS MODEL 2600 PEDIATRIC PULMOONARY CART is BZC.

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: BZC)

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.

K240293STSTechbopulm, Ltd.K183567Vyntus/SentrySuite Product LineVyaire MedicalK190853Vyntus BODYVyaire Medical, Inc.K181524Vyntus ONE with CART, Vyntus ONE PFT only with CART, Vyntus ONE with adjustable CART, Vyntus ONE PFT only with adjustable CARTVyaire Medical, Inc.K162515COSMED K5 Wearable Metabolic TechnologyCosmed SrlK161295MiniBox +Pulmone Advanced Medical Devices, Ltd.

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.

↑