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FDA 510(k)

IV ADMINISTRATION SET B400 SP

K-Number: K042693 · 2004-10-21

Decision Date2004-10-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV ADMINISTRATION SET B400 SP is the device name listed in this FDA 510(k) record. The listed applicant is Codan US Corp.. It received FDA 510(k) clearance on 2004-10-21 under 510(k) number K042693. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV ADMINISTRATION SET B400 SP?

IV ADMINISTRATION SET B400 SP is a medical device that received FDA 510(k) clearance on 2004-10-21. The listed applicant is Codan US Corp.. The 510(k) number is K042693.

When did IV ADMINISTRATION SET B400 SP receive FDA 510(k) clearance?

IV ADMINISTRATION SET B400 SP received FDA 510(k) clearance on 2004-10-21, under 510(k) number K042693.

Who is the listed applicant for IV ADMINISTRATION SET B400 SP?

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

What is the FDA product code for IV ADMINISTRATION SET B400 SP?

The FDA product code for IV ADMINISTRATION SET B400 SP is FPA.

Related Clinical Trials

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.

Other records listing Codan US Corp. 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.

View all 7 devices →

Related Devices (Code: FPA)

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.

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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