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FDA 510(k)

MODIFICATION OF MOSS P.E.G. TRAY

K-Number: K984628 · 1999-03-17

ApplicantMoss Tubes, Inc.
Decision Date1999-03-17
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF MOSS P.E.G. TRAY 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 1999-03-17 under 510(k) number K984628. 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 MODIFICATION OF MOSS P.E.G. TRAY?

MODIFICATION OF MOSS P.E.G. TRAY is a medical device that received FDA 510(k) clearance on 1999-03-17. The listed applicant is Moss Tubes, Inc.. The 510(k) number is K984628.

When did MODIFICATION OF MOSS P.E.G. TRAY receive FDA 510(k) clearance?

MODIFICATION OF MOSS P.E.G. TRAY received FDA 510(k) clearance on 1999-03-17, under 510(k) number K984628.

Who is the listed applicant for MODIFICATION OF MOSS P.E.G. TRAY?

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 MODIFICATION OF MOSS P.E.G. TRAY?

The FDA product code for MODIFICATION OF MOSS P.E.G. 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.

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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 TUBEK984629MOSS TUBES, INC. NASAL TUBE - MARK IVK984310MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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