BLOOD PUMP MODEL 7000
K-Number: K780942 · 1978-06-19
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Device Summary
Frequently Asked Questions
What is the BLOOD PUMP MODEL 7000?
BLOOD PUMP MODEL 7000 is a medical device that received FDA 510(k) clearance on 1978-06-19. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K780942.
When did BLOOD PUMP MODEL 7000 receive FDA 510(k) clearance?
BLOOD PUMP MODEL 7000 received FDA 510(k) clearance on 1978-06-19, under 510(k) number K780942.
Who is the listed applicant for BLOOD PUMP MODEL 7000?
The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD PUMP MODEL 7000?
The FDA product code for BLOOD PUMP MODEL 7000 is DWB.
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 3M Health Care, Sarns 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: DWB)
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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