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FDA 510(k)

ENTERAL FEEDING BAG, 1000 ML, & TUBING SET

K-Number: K851975 · 1985-09-05

ApplicantVenusa , Ltd.
Decision Date1985-09-05
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL FEEDING BAG, 1000 ML, & TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Venusa , Ltd.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K851975. 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 ENTERAL FEEDING BAG, 1000 ML, & TUBING SET?

ENTERAL FEEDING BAG, 1000 ML, & TUBING SET is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Venusa , Ltd.. The 510(k) number is K851975.

When did ENTERAL FEEDING BAG, 1000 ML, & TUBING SET receive FDA 510(k) clearance?

ENTERAL FEEDING BAG, 1000 ML, & TUBING SET received FDA 510(k) clearance on 1985-09-05, under 510(k) number K851975.

Who is the listed applicant for ENTERAL FEEDING BAG, 1000 ML, & TUBING SET?

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

What is the FDA product code for ENTERAL FEEDING BAG, 1000 ML, & TUBING SET?

The FDA product code for ENTERAL FEEDING BAG, 1000 ML, & TUBING SET is KNT.

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Other records listing Venusa , 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.

K994429VENUSA, LTD. EXTENSION SET WITH FILTERK981683HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01YK905518BERLEX BOLUS/INFUSION(TM) INTRAVENOUS ADMIN SETK843692FLU VEN I.V. SET 0153-C PERMA-SETK842088FLU MET 2K812981FLUVEN SETS (EXT-1, EXT-2, EXT-3, EXT-4)

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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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