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FDA 510(k)

Y2K2 ENTERNAL TUBE FLUID FILTER

K-Number: K051206 · 2005-11-02

ApplicantMoss Medical Products
Decision Date2005-11-02
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Y2K2 ENTERNAL TUBE FLUID FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Moss Medical Products. It received FDA 510(k) clearance on 2005-11-02 under 510(k) number K051206. 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 Y2K2 ENTERNAL TUBE FLUID FILTER?

Y2K2 ENTERNAL TUBE FLUID FILTER is a medical device that received FDA 510(k) clearance on 2005-11-02. The listed applicant is Moss Medical Products. The 510(k) number is K051206.

When did Y2K2 ENTERNAL TUBE FLUID FILTER receive FDA 510(k) clearance?

Y2K2 ENTERNAL TUBE FLUID FILTER received FDA 510(k) clearance on 2005-11-02, under 510(k) number K051206.

Who is the listed applicant for Y2K2 ENTERNAL TUBE FLUID FILTER?

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

What is the FDA product code for Y2K2 ENTERNAL TUBE FLUID FILTER?

The FDA product code for Y2K2 ENTERNAL TUBE FLUID FILTER is KNT.

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Other records listing Moss Medical Products 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.

K030413Y2K2 ENTERNAL FEEDING MANAGERK031492MOSSMED DUAL INTERMITTENT ASPIRATORK913701MOSS - ANCHOR SETK910910MOSS- ANCHOR SETK910912MOSS NASAL TUBE MARK IVK910911MOSS P.E.G. TRAY

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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.

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