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FDA 510(k)

MEDCOMP SC4

K-Number: K022678 · 2003-02-24

ApplicantMedcomp
Decision Date2003-02-24
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

MEDCOMP SC4 is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp. It received FDA 510(k) clearance on 2003-02-24 under 510(k) number K022678. 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 MEDCOMP SC4?

MEDCOMP SC4 is a medical device that received FDA 510(k) clearance on 2003-02-24. The listed applicant is Medcomp. The 510(k) number is K022678.

When did MEDCOMP SC4 receive FDA 510(k) clearance?

MEDCOMP SC4 received FDA 510(k) clearance on 2003-02-24, under 510(k) number K022678.

Who is the listed applicant for MEDCOMP SC4?

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 MEDCOMP SC4?

The FDA product code for MEDCOMP SC4 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.

K123292T3K1029662.6F X 20CM VASCU-PICC, 2.6F X 50CM VASCU-PICCK091954MICRO-STICK SETK091953PRO-PICCK092347PRO-PICC CTK090394VALVED TEARWAY INTRODUCER

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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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