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FDA 510(k)

DOBBHOFF DUAL PORT FEEDING TUBE

K-Number: K112511 · 2012-05-11

ApplicantCovidien Lp, Formerly Registered AS Kendall
Decision Date2012-05-11
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DOBBHOFF DUAL PORT FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Covidien Lp, Formerly Registered AS Kendall. It received FDA 510(k) clearance on 2012-05-11 under 510(k) number K112511. 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 DOBBHOFF DUAL PORT FEEDING TUBE?

DOBBHOFF DUAL PORT FEEDING TUBE is a medical device that received FDA 510(k) clearance on 2012-05-11. The listed applicant is Covidien Lp, Formerly Registered AS Kendall. The 510(k) number is K112511.

When did DOBBHOFF DUAL PORT FEEDING TUBE receive FDA 510(k) clearance?

DOBBHOFF DUAL PORT FEEDING TUBE received FDA 510(k) clearance on 2012-05-11, under 510(k) number K112511.

Who is the listed applicant for DOBBHOFF DUAL PORT FEEDING TUBE?

The FDA 510(k) record lists Covidien Lp, Formerly Registered AS Kendall as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOBBHOFF DUAL PORT FEEDING TUBE?

The FDA product code for DOBBHOFF DUAL PORT FEEDING TUBE is KNT.

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Other records listing Covidien Lp, Formerly Registered AS Kendall 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.

K130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.K092205PALINDROME P HEMODIALYSIS 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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