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FDA 510(k)

IV PUMP FILTERSET, UNIVERSAL

K-Number: K770843 · 1977-06-14

ApplicantAbbott Laboratories
Decision Date1977-06-14
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV PUMP FILTERSET, UNIVERSAL is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1977-06-14 under 510(k) number K770843. 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 IV PUMP FILTERSET, UNIVERSAL?

IV PUMP FILTERSET, UNIVERSAL is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is Abbott Laboratories. The 510(k) number is K770843.

When did IV PUMP FILTERSET, UNIVERSAL receive FDA 510(k) clearance?

IV PUMP FILTERSET, UNIVERSAL received FDA 510(k) clearance on 1977-06-14, under 510(k) number K770843.

Who is the listed applicant for IV PUMP FILTERSET, UNIVERSAL?

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 IV PUMP FILTERSET, UNIVERSAL?

The FDA product code for IV PUMP FILTERSET, UNIVERSAL 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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