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FDA 510(k)

CORD STICK MULTIPLE DRAW SYSTEM

K-Number: K031058 · 2003-06-13

ApplicantCord Stick Corp.
Decision Date2003-06-13
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CORD STICK MULTIPLE DRAW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cord Stick Corp.. It received FDA 510(k) clearance on 2003-06-13 under 510(k) number K031058. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORD STICK MULTIPLE DRAW SYSTEM?

CORD STICK MULTIPLE DRAW SYSTEM is a medical device that received FDA 510(k) clearance on 2003-06-13. The listed applicant is Cord Stick Corp.. The 510(k) number is K031058.

When did CORD STICK MULTIPLE DRAW SYSTEM receive FDA 510(k) clearance?

CORD STICK MULTIPLE DRAW SYSTEM received FDA 510(k) clearance on 2003-06-13, under 510(k) number K031058.

Who is the listed applicant for CORD STICK MULTIPLE DRAW SYSTEM?

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

What is the FDA product code for CORD STICK MULTIPLE DRAW SYSTEM?

The FDA product code for CORD STICK MULTIPLE DRAW SYSTEM is FMI.

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Related Devices (Code: FMI)

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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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.

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