PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE
K-Number: K875095 · 1988-02-29
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Device Summary
Frequently Asked Questions
What is the PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE?
PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE is a medical device that received FDA 510(k) clearance on 1988-02-29. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K875095.
When did PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE receive FDA 510(k) clearance?
PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE received FDA 510(k) clearance on 1988-02-29, under 510(k) number K875095.
Who is the listed applicant for PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE?
The FDA 510(k) record lists Pall Biomedical Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE?
The FDA product code for PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE is JOD.
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 Pall Biomedical Products Co. 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: JOD)
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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