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FDA 510(k)

SECUMAX BLOOD COLLECTION SYSTEM

K-Number: K032141 · 2004-01-28

ApplicantTiger Meditech Incorporated
Decision Date2004-01-28
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SECUMAX BLOOD COLLECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tiger Meditech Incorporated. It received FDA 510(k) clearance on 2004-01-28 under 510(k) number K032141. 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 SECUMAX BLOOD COLLECTION SYSTEM?

SECUMAX BLOOD COLLECTION SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-28. The listed applicant is Tiger Meditech Incorporated. The 510(k) number is K032141.

When did SECUMAX BLOOD COLLECTION SYSTEM receive FDA 510(k) clearance?

SECUMAX BLOOD COLLECTION SYSTEM received FDA 510(k) clearance on 2004-01-28, under 510(k) number K032141.

Who is the listed applicant for SECUMAX BLOOD COLLECTION SYSTEM?

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

What is the FDA product code for SECUMAX BLOOD COLLECTION SYSTEM?

The FDA product code for SECUMAX BLOOD COLLECTION 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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