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FDA 510(k)

FOOTPRINT MEDICAL SILICONE FEEDING TUBE

K-Number: K090559 · 2009-05-04

ApplicantFootprint Medical
Decision Date2009-05-04
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FOOTPRINT MEDICAL SILICONE FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Footprint Medical. It received FDA 510(k) clearance on 2009-05-04 under 510(k) number K090559. 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 FOOTPRINT MEDICAL SILICONE FEEDING TUBE?

FOOTPRINT MEDICAL SILICONE FEEDING TUBE is a medical device that received FDA 510(k) clearance on 2009-05-04. The listed applicant is Footprint Medical. The 510(k) number is K090559.

When did FOOTPRINT MEDICAL SILICONE FEEDING TUBE receive FDA 510(k) clearance?

FOOTPRINT MEDICAL SILICONE FEEDING TUBE received FDA 510(k) clearance on 2009-05-04, under 510(k) number K090559.

Who is the listed applicant for FOOTPRINT MEDICAL SILICONE FEEDING TUBE?

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

What is the FDA product code for FOOTPRINT MEDICAL SILICONE FEEDING TUBE?

The FDA product code for FOOTPRINT MEDICAL SILICONE FEEDING TUBE is KNT.

Related Clinical Trials

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Other records listing Footprint Medical 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.

K093026FOOTPRINT MEDICAL 1.9 FR PICC INTRODUCERK091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENK091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERK091488FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER, MODEL S1PIC1.9-CK090576FOOTPRINT URINARY DRAINAGE CATHETER

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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