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)

ENDOTRACHEAL TUBE CHANGERS

K-Number: K102127 · 2010-08-27

ApplicantInstrumentation Industries, Inc.
Decision Date2010-08-27
Product CodeLNZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENDOTRACHEAL TUBE CHANGERS is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 2010-08-27 under 510(k) number K102127. The device is classified under product code LNZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOTRACHEAL TUBE CHANGERS?

ENDOTRACHEAL TUBE CHANGERS is a medical device that received FDA 510(k) clearance on 2010-08-27. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K102127.

When did ENDOTRACHEAL TUBE CHANGERS receive FDA 510(k) clearance?

ENDOTRACHEAL TUBE CHANGERS received FDA 510(k) clearance on 2010-08-27, under 510(k) number K102127.

Who is the listed applicant for ENDOTRACHEAL TUBE CHANGERS?

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

What is the FDA product code for ENDOTRACHEAL TUBE CHANGERS?

The FDA product code for ENDOTRACHEAL TUBE CHANGERS is LNZ.

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 Instrumentation Industries, 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.

K180510NS 120P-TRS Airway Pressure GaugeK162753RTC 26-C Inline Aerosol AdapterK113644PILOT TUBE REPAIR KITK101857RTC-24 VP METERED DOSE INHALER ADAPTER, MODEL RTC 24-VK091111RTC METERED DOSE INHALER ADAPTERS-SINGLE PATIENT USE, MODEL RTC 24-V, RTC MDI ADAPTER KIT-SINGLE PATIENT USE, MODEL RTCK081778NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS

View all 45 devices →

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.

↑