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)

K-TUBE

K-Number: K844745 · 1985-01-07

ApplicantMidwest Metabolic Support Group
Decision Date1985-01-07
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

K-TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Metabolic Support Group. It received FDA 510(k) clearance on 1985-01-07 under 510(k) number K844745. 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 K-TUBE?

K-TUBE is a medical device that received FDA 510(k) clearance on 1985-01-07. The listed applicant is Midwest Metabolic Support Group. The 510(k) number is K844745.

When did K-TUBE receive FDA 510(k) clearance?

K-TUBE received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844745.

Who is the listed applicant for K-TUBE?

The FDA 510(k) record lists Midwest Metabolic Support Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K-TUBE?

The FDA product code for K-TUBE is KNT.

Other records listing Midwest Metabolic Support Group 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.

K843939PEDIATRIC SIZE K-TUBE A OR BK840019K-TUBE REPAIR KITK813504ACESSORY TO MODIFIED FREEDING JEJUNOSTO

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.

↑