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FDA 510(k)

AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET

K-Number: K120272 · 2012-02-17

ApplicantKentec Medical, Inc.
Decision Date2012-02-17
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Kentec Medical, Inc.. It received FDA 510(k) clearance on 2012-02-17 under 510(k) number K120272. 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 AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET?

AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET is a medical device that received FDA 510(k) clearance on 2012-02-17. The listed applicant is Kentec Medical, Inc.. The 510(k) number is K120272.

When did AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET receive FDA 510(k) clearance?

AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET received FDA 510(k) clearance on 2012-02-17, under 510(k) number K120272.

Who is the listed applicant for AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET?

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

What is the FDA product code for AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET?

The FDA product code for AMERITUS MEDICAL ENTERAL FEEDING EXTENSION SET is KNT.

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Other records listing Kentec Medical, 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.

K100526AMERITUS ENTRAL (TM) ENTERAL FEEDING TUBEK050443ACCU-LEADK970686ACCUTEMP-PROBEK960080ACCUTEMP PROBEK853475GRAM-MA NEONATAL SC

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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