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FDA 510(k)

IVEX-TPN EXTENSION FILTER SET

K-Number: K913308 · 1992-01-15

ApplicantAbbott Laboratories
Decision Date1992-01-15
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVEX-TPN EXTENSION FILTER SET is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1992-01-15 under 510(k) number K913308. 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 IVEX-TPN EXTENSION FILTER SET?

IVEX-TPN EXTENSION FILTER SET is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Abbott Laboratories. The 510(k) number is K913308.

When did IVEX-TPN EXTENSION FILTER SET receive FDA 510(k) clearance?

IVEX-TPN EXTENSION FILTER SET received FDA 510(k) clearance on 1992-01-15, under 510(k) number K913308.

Who is the listed applicant for IVEX-TPN EXTENSION FILTER SET?

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

What is the FDA product code for IVEX-TPN EXTENSION FILTER SET?

The FDA product code for IVEX-TPN EXTENSION FILTER SET is FPB.

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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.K993379PALL SUPOR AEF FILTERPall Corp.K9746610.2 U BACTERIAL FILTERSims Deltec, Inc.

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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