AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET
K-Number: K912069 · 1993-10-14
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Device Summary
Frequently Asked Questions
What is the AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET?
AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET is a medical device that received FDA 510(k) clearance on 1993-10-14. The listed applicant is 3M Avi, Inc.. The 510(k) number is K912069.
When did AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET receive FDA 510(k) clearance?
AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET received FDA 510(k) clearance on 1993-10-14, under 510(k) number K912069.
Who is the listed applicant for AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET?
The FDA 510(k) record lists 3M Avi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET?
The FDA product code for AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET 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 3M Avi, 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: 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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