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FDA 510(k)

MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R

K-Number: K013988 · 2002-04-04

Decision Date2002-04-04
Product CodeBSN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 2002-04-04 under 510(k) number K013988. 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 GP STERILIZING FILTER UNIT, MODEL SLGP 033 R?

MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R is a medical device that received FDA 510(k) clearance on 2002-04-04. The listed applicant is Millipore Corp.. The 510(k) number is K013988.

When did MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R receive FDA 510(k) clearance?

MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R received FDA 510(k) clearance on 2002-04-04, under 510(k) number K013988.

Who is the listed applicant for MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R?

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 GP STERILIZING FILTER UNIT, MODEL SLGP 033 R?

The FDA product code for MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R is BSN.

Related Clinical Trials

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.

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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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