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)

THORACIC CATHETER (CHEST DRAINAGE TUBE)

K-Number: K863142 · 1986-08-29

ApplicantSheridan Catheter Corp.
Decision Date1986-08-29
Product CodeGBS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THORACIC CATHETER (CHEST DRAINAGE TUBE) 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 1986-08-29 under 510(k) number K863142. The device is classified under product code GBS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORACIC CATHETER (CHEST DRAINAGE TUBE)?

THORACIC CATHETER (CHEST DRAINAGE TUBE) is a medical device that received FDA 510(k) clearance on 1986-08-29. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K863142.

When did THORACIC CATHETER (CHEST DRAINAGE TUBE) receive FDA 510(k) clearance?

THORACIC CATHETER (CHEST DRAINAGE TUBE) received FDA 510(k) clearance on 1986-08-29, under 510(k) number K863142.

Who is the listed applicant for THORACIC CATHETER (CHEST DRAINAGE TUBE)?

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 THORACIC CATHETER (CHEST DRAINAGE TUBE)?

The FDA product code for THORACIC CATHETER (CHEST DRAINAGE TUBE) is GBS.

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: GBS)

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.

K912645ATRIUMS PDR THORACIC CATHETERAtrium Medical Corp.K883887AXIOM ATRAUM WOUND DRAINSAxiom, Inc.K881873INTRODUCTION/DRAINAGE CATHETER & ACCESSSheridan Catheter Corp.K880895URESIL WOUND DRAIN TROCARUresil Corp.K880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPGenesis Industries, Inc.K873377CLOSED CHEST DRAINAGE SET W/SUTURESGish Biomedical, 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.

↑