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FDA 510(k)

MICROTEC BACTERIAL FILTER

K-Number: K790407 · 1979-05-16

ApplicantMedex, Inc.
Decision Date1979-05-16
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROTEC BACTERIAL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1979-05-16 under 510(k) number K790407. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTEC BACTERIAL FILTER?

MICROTEC BACTERIAL FILTER is a medical device that received FDA 510(k) clearance on 1979-05-16. The listed applicant is Medex, Inc.. The 510(k) number is K790407.

When did MICROTEC BACTERIAL FILTER receive FDA 510(k) clearance?

MICROTEC BACTERIAL FILTER received FDA 510(k) clearance on 1979-05-16, under 510(k) number K790407.

Who is the listed applicant for MICROTEC BACTERIAL FILTER?

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

What is the FDA product code for MICROTEC BACTERIAL FILTER?

The FDA product code for MICROTEC BACTERIAL FILTER is DRS.

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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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