AMBIT CONTINUOUS AMBULATORY INFUSION PUMP
K-Number: K033325 · 2003-11-06
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Device Summary
Frequently Asked Questions
What is the AMBIT CONTINUOUS AMBULATORY INFUSION PUMP?
AMBIT CONTINUOUS AMBULATORY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2003-11-06. The listed applicant is Sorenson Medical, Inc.. The 510(k) number is K033325.
When did AMBIT CONTINUOUS AMBULATORY INFUSION PUMP receive FDA 510(k) clearance?
AMBIT CONTINUOUS AMBULATORY INFUSION PUMP received FDA 510(k) clearance on 2003-11-06, under 510(k) number K033325.
Who is the listed applicant for AMBIT CONTINUOUS AMBULATORY INFUSION PUMP?
The FDA 510(k) record lists Sorenson Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMBIT CONTINUOUS AMBULATORY INFUSION PUMP?
The FDA product code for AMBIT CONTINUOUS AMBULATORY INFUSION PUMP 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 Sorenson Medical, 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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