FDA 510(k)

REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY

K-Number: K954776 · 1996-01-22

ApplicantUnited States Endoscopy Group, Inc.

Decision Date1996-01-22

Product CodeKNT

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1996-01-22 under 510(k) number K954776. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY?

REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1996-01-22. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K954776.

When did REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY receive FDA 510(k) clearance?

REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY received FDA 510(k) clearance on 1996-01-22, under 510(k) number K954776.

Who is the listed applicant for REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY?

The FDA product code for REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY is KNT.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing United States Endoscopy Group, Inc. as applicant

K192265gi-4000 Electrosurgical Generator K200745Lariat, Hot/Cold Snare K192059Bio Guard Air/Water & Suction Valves K191559AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM K182909Roth Net Retriever Product Line K182258AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - Fujifilm

View all 85 devices →

Related Devices (Code: KNT)

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLC K253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)C.R. Bard, Inc.K250389XNY Disposable Gastric Calibration TubeChangzhou Xin Neng Yuan Medical Stapler Co.,Ltd K243228Flexi-Seal AIR (with ENFit Connector)Convatec K242336hygh-tec Drainage IIAmb Medtec K242901ZZIREN™ Orogastric Tube; ZZIREN™ SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN™ SGT Orogastric Tube - 36 Fr (ZZ-SGT-36); ZZIREN™ SGT Orogastric Tube - 40 Fr (ZZ-SGT-40); ZZIREN™ GBT Orogastric Tube - 32 Fr (ZZ-GBT-32); ZZIREN™ GBT Orogastric Tube - 36 Fr (ZZ-GBT-36); ZZIREN™ GBT Orogastric Tube - 40 Fr (ZZ-GBT-40)Tools For Surgery, LLC

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.