BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR
K-Number: K954850 · 1996-10-30
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Device Summary
Frequently Asked Questions
What is the BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR?
BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR is a medical device that received FDA 510(k) clearance on 1996-10-30. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K954850.
When did BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR receive FDA 510(k) clearance?
BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR received FDA 510(k) clearance on 1996-10-30, under 510(k) number K954850.
Who is the listed applicant for BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR?
The FDA product code for BARD WILLIAM HARVEY HF-6000 MEMBRANE OXYGENATOR is DTZ.
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 C.R. Bard, 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: DTZ)
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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