FDA 510(k)

End Cap

K-Number: K210461 · 2021-09-14

ApplicantMedical Components Inc (Medcomp)

Decision Date2021-09-14

Product CodeMSD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

End Cap is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components Inc (Medcomp). It received FDA 510(k) clearance on 2021-09-14 under 510(k) number K210461. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the End Cap?

End Cap is a medical device that received FDA 510(k) clearance on 2021-09-14. The listed applicant is Medical Components Inc (Medcomp). The 510(k) number is K210461.

When did End Cap receive FDA 510(k) clearance?

End Cap received FDA 510(k) clearance on 2021-09-14, under 510(k) number K210461.

Who is the listed applicant for End Cap?

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

What is the FDA product code for End Cap?

The FDA product code for End Cap is MSD.

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 Corporation 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.K202176Symetrex LTHD Catheter, Symetrex LTHD Catheter with SideholesMedical Components, Inc. (dba MedComp)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.