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FDA 510(k)

OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20

K-Number: K921179 · 1993-03-29

ApplicantKeymed, Inc.
Decision Date1993-03-29
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20 is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1993-03-29 under 510(k) number K921179. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20?

OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20 is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Keymed, Inc.. The 510(k) number is K921179.

When did OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20 receive FDA 510(k) clearance?

OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20 received FDA 510(k) clearance on 1993-03-29, under 510(k) number K921179.

Who is the listed applicant for OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20?

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

What is the FDA product code for OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20?

The FDA product code for OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20 is FEB.

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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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