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FDA 510(k)

DIETO CONTAINER FOR ENTERNAL NUTRIT

K-Number: K840916 · 1984-04-04

ApplicantGil-Med Industries C/O Kegan & Kegan, Ltd.
Decision Date1984-04-04
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIETO CONTAINER FOR ENTERNAL NUTRIT is the device name listed in this FDA 510(k) record. The listed applicant is Gil-Med Industries C/O Kegan & Kegan, Ltd.. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K840916. 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 DIETO CONTAINER FOR ENTERNAL NUTRIT?

DIETO CONTAINER FOR ENTERNAL NUTRIT is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Gil-Med Industries C/O Kegan & Kegan, Ltd.. The 510(k) number is K840916.

When did DIETO CONTAINER FOR ENTERNAL NUTRIT receive FDA 510(k) clearance?

DIETO CONTAINER FOR ENTERNAL NUTRIT received FDA 510(k) clearance on 1984-04-04, under 510(k) number K840916.

Who is the listed applicant for DIETO CONTAINER FOR ENTERNAL NUTRIT?

The FDA 510(k) record lists Gil-Med Industries C/O Kegan & Kegan, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIETO CONTAINER FOR ENTERNAL NUTRIT?

The FDA product code for DIETO CONTAINER FOR ENTERNAL NUTRIT is KNT.

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Other records listing Gil-Med Industries C/O Kegan & Kegan, Ltd. 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.

K880506MODIFIED EVA-MIX AND DI-MIX BAGSK870274DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINERK861862DIETO CONTAINER FOR ENTERAL NUTRITIONK841597GIL-MED PARENTERAL NUTRITION OR MEDICINEK841224URO-MALE INCONTINENCE CATHETERK840915DIMIX CONTAINER FOR PARNETERAL NUTRIT

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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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