ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP
K-Number: K894255 · 1989-09-26
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Device Summary
Frequently Asked Questions
What is the ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP?
ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is St. Jude Medical, Inc.. The 510(k) number is K894255.
When did ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP receive FDA 510(k) clearance?
ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP received FDA 510(k) clearance on 1989-09-26, under 510(k) number K894255.
Who is the listed applicant for ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP?
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 ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP?
The FDA product code for ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP 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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