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)

AMT G-J TUBE

K-Number: K110804 · 2011-10-19

ApplicantApplied Medical Technology, Inc.
Decision Date2011-10-19
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

AMT G-J TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2011-10-19 under 510(k) number K110804. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the AMT G-J TUBE?

AMT G-J TUBE is a medical device that received FDA 510(k) clearance on 2011-10-19. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K110804.

When did AMT G-J TUBE receive FDA 510(k) clearance?

AMT G-J TUBE received FDA 510(k) clearance on 2011-10-19, under 510(k) number K110804.

Who is the listed applicant for AMT G-J TUBE?

The FDA 510(k) record lists Applied Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMT G-J TUBE?

The FDA product code for AMT G-J TUBE is KNT.

Other records listing Applied Medical Technology, Inc. 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.

K252438Explant ExpressK240514AMT Low-Profile Suprapubic Catheter & Drainage SetK241111AMT Suture PasserK222846AMT G-Tube Balloon Gastrostomy Feeding DeviceK202539Nutriglide(TM) Nasal Feeding TubeK193612AMT Suture Delivery System

View all 21 devices →

Related Devices (Code: KNT)

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.

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLCK253514Minnesota 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.,LtdK243228Flexi-Seal AIR (with ENFit Connector)ConvatecK242336hygh-tec Drainage IIAmb MedtecK242901ZZIREN™ 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.

↑