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FDA 510(k)

ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403

K-Number: K844203 · 1985-01-02

ApplicantExco, Inc.
Decision Date1985-01-02
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403 is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1985-01-02 under 510(k) number K844203. 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 ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403?

ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403 is a medical device that received FDA 510(k) clearance on 1985-01-02. The listed applicant is Exco, Inc.. The 510(k) number is K844203.

When did ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403 receive FDA 510(k) clearance?

ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403 received FDA 510(k) clearance on 1985-01-02, under 510(k) number K844203.

Who is the listed applicant for ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403?

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

What is the FDA product code for ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403?

The FDA product code for ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403 is KNT.

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Other records listing Exco, 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.

K844175ENTERNAL FEEDING TUBE-POLYURETHANE EF504K844174FLEXIBLE STAINLESS STEEL STYLET FOR ENTERNAL FEEDIK832628VYGON THORACIC DRAINAGE-VARIOUS #'SK831802LIFE VAC #2191 & 2192K833079CENTRACATH #130,135 & 137-HEMOCATH #K830910MANOMETER SET C.V.P. #S 298/299

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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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