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FDA 510(k)

XRO UMBILICAL CATHETER-CODE 270

K-Number: K851005 · 1985-05-21

ApplicantVygon Corp.
Decision Date1985-05-21
Product CodeFOS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

XRO UMBILICAL CATHETER-CODE 270 is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1985-05-21 under 510(k) number K851005. The device is classified under product code FOS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XRO UMBILICAL CATHETER-CODE 270?

XRO UMBILICAL CATHETER-CODE 270 is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Vygon Corp.. The 510(k) number is K851005.

When did XRO UMBILICAL CATHETER-CODE 270 receive FDA 510(k) clearance?

XRO UMBILICAL CATHETER-CODE 270 received FDA 510(k) clearance on 1985-05-21, under 510(k) number K851005.

Who is the listed applicant for XRO UMBILICAL CATHETER-CODE 270?

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 UMBILICAL CATHETER-CODE 270?

The FDA product code for XRO UMBILICAL CATHETER-CODE 270 is FOS.

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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: FOS)

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.

K201697Umbilical Vessels CatheterHaolang Medical USA CorporationK130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Covidien Lp, Formerly Registered AS KendallK120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETERFootprint Medical, Inc.K091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERFootprint MedicalK091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENFootprint MedicalK081515NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0Neomed, Inc.

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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