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FDA 510(k)

MICROFLOW

K-Number: K924684 · 1992-12-15

ApplicantMountain Medical Equipment, Inc.
Decision Date1992-12-15
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICROFLOW is the device name listed in this FDA 510(k) record. The listed applicant is Mountain Medical Equipment, Inc.. It received FDA 510(k) clearance on 1992-12-15 under 510(k) number K924684. 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 MICROFLOW?

MICROFLOW is a medical device that received FDA 510(k) clearance on 1992-12-15. The listed applicant is Mountain Medical Equipment, Inc.. The 510(k) number is K924684.

When did MICROFLOW receive FDA 510(k) clearance?

MICROFLOW received FDA 510(k) clearance on 1992-12-15, under 510(k) number K924684.

Who is the listed applicant for MICROFLOW?

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

What is the FDA product code for MICROFLOW?

The FDA product code for MICROFLOW is CAF.

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Other records listing Mountain Medical Equipment, Inc. as applicant

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K941793OXYGEN CONCENTRATION STATUS INDICATOR (O.C.S.I.)K923650SCOTTYK914916ALPINE VK902890ASPEN 3 OXYGEN CONCENTRATORK893531CUFF SPECULUMK884084PORTABLE OXYGEN GENERATOR

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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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