AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS
K-Number: K912738 · 1991-08-12
Advertisement
Device Summary
Frequently Asked Questions
What is the AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS?
AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1991-08-12. The listed applicant is 3M Avi, Inc.. The 510(k) number is K912738.
When did AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS receive FDA 510(k) clearance?
AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS received FDA 510(k) clearance on 1991-08-12, under 510(k) number K912738.
Who is the listed applicant for AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS?
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 VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS?
The FDA product code for AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS is FRN.
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: FRN)
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.
Advertisement