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FDA 510(k)

14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55

K-Number: K021759 · 2002-08-27

ApplicantMedcomp
Decision Date2002-08-27
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55 is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp. It received FDA 510(k) clearance on 2002-08-27 under 510(k) number K021759. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the 14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55?

14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55 is a medical device that received FDA 510(k) clearance on 2002-08-27. The listed applicant is Medcomp. The 510(k) number is K021759.

When did 14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55 receive FDA 510(k) clearance?

14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55 received FDA 510(k) clearance on 2002-08-27, under 510(k) number K021759.

Who is the listed applicant for 14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55?

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

What is the FDA product code for 14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55?

The FDA product code for 14F X 55CM ULTRA-FLOW CATHETER, MODELS UFS55, UFT55 is MSD.

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Other records listing Medcomp 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.

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Related Devices (Code: MSD)

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.

K241581Hemodialysis CatheterHaolang Medical USA CorporationK210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro Long-Term Hemodialysis CatheterC.R. Bard, Inc.K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B Bard, Inc.K202150GlidePath 7.5F Long-Term Dialysis CatheterC.R. Bard, 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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