LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI
K-Number: K933014 · 1994-09-28
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Device Summary
Frequently Asked Questions
What is the LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI?
LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI is a medical device that received FDA 510(k) clearance on 1994-09-28. The listed applicant is St. Jude Medical, Inc.. The 510(k) number is K933014.
When did LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI receive FDA 510(k) clearance?
LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI received FDA 510(k) clearance on 1994-09-28, under 510(k) number K933014.
Who is the listed applicant for LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI?
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 CENTRIFUGEL PUMP INTERFACE #210PI?
The FDA product code for LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI 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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