MULTI-DRIP INFUSION CATHETER
K-Number: K042246 · 2004-08-31
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Device Summary
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
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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