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)

TRACHEOBRONCHIAL SUCTION CATHETER

K-Number: K864468 · 1987-01-06

ApplicantSheridan Catheter Corp.
Decision Date1987-01-06
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRACHEOBRONCHIAL SUCTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Sheridan Catheter Corp.. It received FDA 510(k) clearance on 1987-01-06 under 510(k) number K864468. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACHEOBRONCHIAL SUCTION CATHETER?

TRACHEOBRONCHIAL SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K864468.

When did TRACHEOBRONCHIAL SUCTION CATHETER receive FDA 510(k) clearance?

TRACHEOBRONCHIAL SUCTION CATHETER received FDA 510(k) clearance on 1987-01-06, under 510(k) number K864468.

Who is the listed applicant for TRACHEOBRONCHIAL SUCTION CATHETER?

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

What is the FDA product code for TRACHEOBRONCHIAL SUCTION CATHETER?

The FDA product code for TRACHEOBRONCHIAL SUCTION CATHETER is BSY.

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 Sheridan Catheter 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.

K922894LAZER-TRACH TRACHEAL TUBEK897046LASER RESISTANT TRACHEAL TUBEK890823ACCESSORY TO CLINICAL ELECTRONIC THERMOMETERK884765CLINICAL ELECTRONIC THERMOMETERSK882918KIM NASO-INTESTINAL TUBEK882127CLINICAL ELECTRONIC THERMOMETERS

View all 39 devices →

Related Devices (Code: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., 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.

↑