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FDA 510(k)

14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL

K-Number: K020315 · 2002-05-24

ApplicantMedcomp
Decision Date2002-05-24
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp. It received FDA 510(k) clearance on 2002-05-24 under 510(k) number K020315. 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 ASH SPLIT-CATH XL, MODEL ASPC55-XL?

14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL is a medical device that received FDA 510(k) clearance on 2002-05-24. The listed applicant is Medcomp. The 510(k) number is K020315.

When did 14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL receive FDA 510(k) clearance?

14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL received FDA 510(k) clearance on 2002-05-24, under 510(k) number K020315.

Who is the listed applicant for 14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL?

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 ASH SPLIT-CATH XL, MODEL ASPC55-XL?

The FDA product code for 14F X 55CM ASH SPLIT-CATH XL, MODEL ASPC55-XL is MSD.

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Other records listing Medcomp as applicant

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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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