LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP
K-Number: K921550 · 1992-05-21
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Device Summary
Frequently Asked Questions
What is the LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP?
LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP is a medical device that received FDA 510(k) clearance on 1992-05-21. The listed applicant is St. Jude Medical, Inc.. The 510(k) number is K921550.
When did LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP receive FDA 510(k) clearance?
LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP received FDA 510(k) clearance on 1992-05-21, under 510(k) number K921550.
Who is the listed applicant for LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP?
The FDA 510(k) record lists St. Jude Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP?
The FDA product code for LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP is KFM.
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 St. Jude 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: KFM)
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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