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FDA 510(k)

XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE

K-Number: K860285 · 1986-02-11

ApplicantVygon Corp.
Decision Date1986-02-11
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1986-02-11 under 510(k) number K860285. 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 XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE?

XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE is a medical device that received FDA 510(k) clearance on 1986-02-11. The listed applicant is Vygon Corp.. The 510(k) number is K860285.

When did XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE receive FDA 510(k) clearance?

XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE received FDA 510(k) clearance on 1986-02-11, under 510(k) number K860285.

Who is the listed applicant for XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE?

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

What is the FDA product code for XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE?

The FDA product code for XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE is KNT.

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Other records listing Vygon Corp. 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.

K121105NUTRISAFE 2 FEEDING TUBEK100163NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXXK073493HEPATOSTAT SETK070705MODIFICATION TO: LATEX-FREE BIONECTOR, MODEL# 896.019, 896.039K061796HEPATOSTAT SET, MODEL 760XK061250MULTICATH EXPERT

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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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