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FDA 510(k)

MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)

K-Number: K963717 · 1997-06-10

ApplicantMillipore Corp.
Decision Date1997-06-10
Product CodeBSN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS) is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1997-06-10 under 510(k) number K963717. The device is classified under product code BSN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)?

MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS) is a medical device that received FDA 510(k) clearance on 1997-06-10. The listed applicant is Millipore Corp.. The 510(k) number is K963717.

When did MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS) receive FDA 510(k) clearance?

MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS) received FDA 510(k) clearance on 1997-06-10, under 510(k) number K963717.

Who is the listed applicant for MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)?

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 MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)?

The FDA product code for MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS) is BSN.

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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 RK941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDAK922388WATERS(TM) LC MODULE I FOR CLINICAL USE

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Related Devices (Code: BSN)

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.

K190663Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6PAJUNK GmbH MedizintechnologieK083451PORTEX EPIDURAL FILTER, MODEL 100/386/010, VARIOUS STANDARD AND CUSTOM TRAYSSmiths Medical Asd, Inc.K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSMillipore Corp.K013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RMillipore Corp.K960928SYRINGEFILTERArbor Technologies, Inc.K902666ANESTHESIA CONDUCTION FILTERArbor Technologies, 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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