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FDA 510(k)

MULTI-DRIP INFUSION CATHETER

K-Number: K042246 · 2004-08-31

Decision Date2004-08-31
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI-DRIP INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Infusion, Inc.. It received FDA 510(k) clearance on 2004-08-31 under 510(k) number K042246. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-DRIP INFUSION CATHETER?

MULTI-DRIP INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 2004-08-31. The listed applicant is Advanced Infusion, Inc.. The 510(k) number is K042246.

When did MULTI-DRIP INFUSION CATHETER receive FDA 510(k) clearance?

MULTI-DRIP INFUSION CATHETER received FDA 510(k) clearance on 2004-08-31, under 510(k) number K042246.

Who is the listed applicant for MULTI-DRIP INFUSION CATHETER?

The FDA 510(k) record lists Advanced Infusion, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-DRIP INFUSION CATHETER?

The FDA product code for MULTI-DRIP INFUSION CATHETER is MEB.

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 Advanced Infusion, Inc. 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.

Related Devices (Code: MEB)

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

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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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