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)

ANAPNOGUARD ENDOTRACHEAL TUBE

K-Number: K093126 · 2010-03-02

ApplicantHospitech Respiration , Ltd.
Decision Date2010-03-02
Product CodeBTP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANAPNOGUARD ENDOTRACHEAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Hospitech Respiration , Ltd.. It received FDA 510(k) clearance on 2010-03-02 under 510(k) number K093126. The device is classified under product code BTP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAPNOGUARD ENDOTRACHEAL TUBE?

ANAPNOGUARD ENDOTRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 2010-03-02. The listed applicant is Hospitech Respiration , Ltd.. The 510(k) number is K093126.

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

ANAPNOGUARD ENDOTRACHEAL TUBE received FDA 510(k) clearance on 2010-03-02, under 510(k) number K093126.

Who is the listed applicant for ANAPNOGUARD ENDOTRACHEAL TUBE?

The FDA 510(k) record lists Hospitech Respiration , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANAPNOGUARD ENDOTRACHEAL TUBE?

The FDA product code for ANAPNOGUARD ENDOTRACHEAL TUBE is BTP.

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 Hospitech Respiration , Ltd. 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.

K221477AG100sK180991AG 100sK150157AnapnoGuard 100 Respiratory Guard SystemK131099AG MASSK122721AG GUFFILL

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.

↑