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)

MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE

K-Number: K984310 · 1999-02-24

ApplicantMoss Tubes, Inc.
Decision Date1999-02-24
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Moss Tubes, Inc.. It received FDA 510(k) clearance on 1999-02-24 under 510(k) number K984310. 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 MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE?

MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE is a medical device that received FDA 510(k) clearance on 1999-02-24. The listed applicant is Moss Tubes, Inc.. The 510(k) number is K984310.

When did MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE receive FDA 510(k) clearance?

MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE received FDA 510(k) clearance on 1999-02-24, under 510(k) number K984310.

Who is the listed applicant for MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE?

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

What is the FDA product code for MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE?

The FDA product code for MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE 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_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 Moss Tubes, 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.

K190414Moss Gastrostomy Tube, Moss Nasal Tube – Mark IVK990389MOSS GASTROSTOMY TUBEK984628MODIFICATION OF MOSS P.E.G. TRAYK984629MOSS TUBES, INC. NASAL TUBE - MARK IV

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.

↑