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FDA 510(k)

MILLIPORE RT-100 AEROSOL RETENTION FILTER

K-Number: K931603 · 1993-05-13

ApplicantSterimatics Co.
Decision Date1993-05-13
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MILLIPORE RT-100 AEROSOL RETENTION FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Sterimatics Co.. It received FDA 510(k) clearance on 1993-05-13 under 510(k) number K931603. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLIPORE RT-100 AEROSOL RETENTION FILTER?

MILLIPORE RT-100 AEROSOL RETENTION FILTER is a medical device that received FDA 510(k) clearance on 1993-05-13. The listed applicant is Sterimatics Co.. The 510(k) number is K931603.

When did MILLIPORE RT-100 AEROSOL RETENTION FILTER receive FDA 510(k) clearance?

MILLIPORE RT-100 AEROSOL RETENTION FILTER received FDA 510(k) clearance on 1993-05-13, under 510(k) number K931603.

Who is the listed applicant for MILLIPORE RT-100 AEROSOL RETENTION FILTER?

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

What is the FDA product code for MILLIPORE RT-100 AEROSOL RETENTION FILTER?

The FDA product code for MILLIPORE RT-100 AEROSOL RETENTION FILTER is CAF.

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Official Source

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