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FDA 510(k)

MILLIPORE IVEX INT FILTER UNIT

K-Number: K832952 · 1983-10-04

ApplicantMillipore Corp.
Decision Date1983-10-04
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MILLIPORE IVEX INT FILTER UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832952. 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 MILLIPORE IVEX INT FILTER UNIT?

MILLIPORE IVEX INT FILTER UNIT is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Millipore Corp.. The 510(k) number is K832952.

When did MILLIPORE IVEX INT FILTER UNIT receive FDA 510(k) clearance?

MILLIPORE IVEX INT FILTER UNIT received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832952.

Who is the listed applicant for MILLIPORE IVEX INT FILTER UNIT?

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

What is the FDA product code for MILLIPORE IVEX INT FILTER UNIT?

The FDA product code for MILLIPORE IVEX INT FILTER UNIT is FPB.

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Other records listing Millipore 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.

K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSK013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDA

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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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