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FDA 510(k)

CHURCHILL 0.22 MICRON LIQUID FILTER SETS

K-Number: K880025 · 1988-04-14

ApplicantChurchill Corp.
Decision Date1988-04-14
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL 0.22 MICRON LIQUID FILTER SETS is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K880025. 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 CHURCHILL 0.22 MICRON LIQUID FILTER SETS?

CHURCHILL 0.22 MICRON LIQUID FILTER SETS is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Churchill Corp.. The 510(k) number is K880025.

When did CHURCHILL 0.22 MICRON LIQUID FILTER SETS receive FDA 510(k) clearance?

CHURCHILL 0.22 MICRON LIQUID FILTER SETS received FDA 510(k) clearance on 1988-04-14, under 510(k) number K880025.

Who is the listed applicant for CHURCHILL 0.22 MICRON LIQUID FILTER SETS?

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

What is the FDA product code for CHURCHILL 0.22 MICRON LIQUID FILTER SETS?

The FDA product code for CHURCHILL 0.22 MICRON LIQUID FILTER SETS is FPB.

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Other records listing Churchill 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.

K880026CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETSK880051ENTERAL BAG/SETK880027CHURCHILL 1.2 MICRON LIQUID FILTER SETK870395CHURCHILL PARENTERAL NUTRITION BAG - EVAK872585CHURCHILL-CATHK872124CHURCHILL ALBUMIN IV ADMINISTRATION SET

View all 35 devices →

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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