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FDA 510(k)

LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE

K-Number: K902518 · 1990-10-16

Decision Date1990-10-16
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE is the device name listed in this FDA 510(k) record. The listed applicant is Pall Biomedical Products Co.. It received FDA 510(k) clearance on 1990-10-16 under 510(k) number K902518. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE?

LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE is a medical device that received FDA 510(k) clearance on 1990-10-16. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K902518.

When did LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE receive FDA 510(k) clearance?

LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE received FDA 510(k) clearance on 1990-10-16, under 510(k) number K902518.

Who is the listed applicant for LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE?

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 LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE?

The FDA product code for LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE is DTM.

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.

View all 28 devices →

Related Devices (Code: DTM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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