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FDA 510(k)

PALL COALESCER

K-Number: K840960 · 1984-03-16

ApplicantPall Biomedical Products Co.
Decision Date1984-03-16
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PALL COALESCER 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 1984-03-16 under 510(k) number K840960. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALL COALESCER?

PALL COALESCER is a medical device that received FDA 510(k) clearance on 1984-03-16. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K840960.

When did PALL COALESCER receive FDA 510(k) clearance?

PALL COALESCER received FDA 510(k) clearance on 1984-03-16, under 510(k) number K840960.

Who is the listed applicant for PALL COALESCER?

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 COALESCER?

The FDA product code for PALL COALESCER is CAH.

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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.

K954331PALL LEA FILTER (LIPID EMULSION FILTER) (I.V. FILTER)K960993PALL SQ40S BLOOD FILTER (SQ40S/SQ40ST)K905794PALL 3N1 FILTERK902518LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICEK884534PALL HEPCHEK (TM) HEPARIN ABSORPTION FILTERK875095PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE

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Related Devices (Code: CAH)

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.

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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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