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)

ENDO-MED TUBE FOR ENDOTRACHEAL MED

K-Number: K810059 · 1981-02-26

ApplicantAckrad Laboratories
Decision Date1981-02-26
Product CodeCCT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENDO-MED TUBE FOR ENDOTRACHEAL MED is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810059. The device is classified under product code CCT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-MED TUBE FOR ENDOTRACHEAL MED?

ENDO-MED TUBE FOR ENDOTRACHEAL MED is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is Ackrad Laboratories. The 510(k) number is K810059.

When did ENDO-MED TUBE FOR ENDOTRACHEAL MED receive FDA 510(k) clearance?

ENDO-MED TUBE FOR ENDOTRACHEAL MED received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810059.

Who is the listed applicant for ENDO-MED TUBE FOR ENDOTRACHEAL MED?

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

What is the FDA product code for ENDO-MED TUBE FOR ENDOTRACHEAL MED?

The FDA product code for ENDO-MED TUBE FOR ENDOTRACHEAL MED is CCT.

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 Ackrad Laboratories 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.

K021272SIB CATHETER, MODEL 61-7005K020954H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAYK020951H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007K970492INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETERK961752H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)K952542ACKRAD ESOPHAGEAL BALLOON CATHETER SET

View all 42 devices →

Related Devices (Code: CCT)

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.

K240114UltraEzAir® (UEA1A)Dualams, Inc., Dba AirkorK172956Medicant Mucosal AtomizerMedica Holdings, LLCK153470MADgic Laryngo-Tracheal Mucosal Atomization DeviceTeleflex MedicalK093584EZ-MISTERN.M. Beale Co., Inc.K070596TOPICAL APPLICATORSharn, Inc.K002255LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)Wolfe Tory Medical, Inc.

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.

↑