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FDA 510(k)

PALL SUPOR AEF FILTER

K-Number: K993379 · 1999-12-16

ApplicantPall Corp.
Decision Date1999-12-16
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PALL SUPOR AEF FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Pall Corp.. It received FDA 510(k) clearance on 1999-12-16 under 510(k) number K993379. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALL SUPOR AEF FILTER?

PALL SUPOR AEF FILTER is a medical device that received FDA 510(k) clearance on 1999-12-16. The listed applicant is Pall Corp.. The 510(k) number is K993379.

When did PALL SUPOR AEF FILTER receive FDA 510(k) clearance?

PALL SUPOR AEF FILTER received FDA 510(k) clearance on 1999-12-16, under 510(k) number K993379.

Who is the listed applicant for PALL SUPOR AEF FILTER?

The FDA 510(k) record lists Pall Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALL SUPOR AEF FILTER?

The FDA product code for PALL SUPOR AEF FILTER is FPB.

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.

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Other records listing Pall Corp. 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.

K022167PALL DONER PRE-EVACUATED POST-OPERATIVE AUTOLOGOUS BLOOD REINFUSION SYSTEMK980762PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICE

Related Devices (Code: FPB)

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.

K261403Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion FilterGlobal Life Sciences Solutions USA, LLCK233277Filter Needle for Single UseHangzhou Qiantang Longyue Biotechnology Co., Ltd.K113227NON-DEHP MICRO-VOLUME EXTENSION SET WITH 0.22 MICRON FILTERBaxter Healthcare CorpK021293ARTERIA BLOOD FILTERArteria Medical Science, Inc.K9746610.2 U BACTERIAL FILTERSims Deltec, Inc.K964283AUTOPRIMEArbor Technologies, Inc.

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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