ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS
K-Number: K993524 · 2000-08-01
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Device Summary
Frequently Asked Questions
What is the ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS?
ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS is a medical device that received FDA 510(k) clearance on 2000-08-01. The listed applicant is Alaris Medical Systems, Inc.. The 510(k) number is K993524.
When did ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS receive FDA 510(k) clearance?
ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS received FDA 510(k) clearance on 2000-08-01, under 510(k) number K993524.
Who is the listed applicant for ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS?
The FDA 510(k) record lists Alaris Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS?
The FDA product code for ADVANTIS ASC INFUSION PUMP AND ADMINISTRATION SETS 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 Alaris Medical Systems, 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.
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