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FDA 510(k)

FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER

K-Number: K932301 · 1993-11-10

ApplicantBaxter Healthcare Corp
Decision Date1993-11-10
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1993-11-10 under 510(k) number K932301. 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 FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER?

FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER is a medical device that received FDA 510(k) clearance on 1993-11-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K932301.

When did FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER receive FDA 510(k) clearance?

FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER received FDA 510(k) clearance on 1993-11-10, under 510(k) number K932301.

Who is the listed applicant for FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER?

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

What is the FDA product code for FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER?

The FDA product code for FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER is FPB.

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Other records listing Baxter Healthcare Corp as applicant

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K190910PrisMax System Version 2K163530PrisMax Control UnitK132734NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND EXTENSION SETSK130245LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH EXTENSION SET, GANG LARGE BORE STOPCOCK MANIFOK123874INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION SETS, CONTINUED, CLEARLINK SYSTEM BURETROL SK123868INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION SETS, SOLUTION SETS, CONTINU-FLO SOLUTION SET

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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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