Olympus-Keymed Disinfectant Fume Extractor DFE-20

FDA 510(k) K921179 · Keymed, Inc.

Substantially Equivalent

510(k) numberK921179

Submission

Device name
Olympus-Keymed Disinfectant Fume Extractor DFE-20
Applicant
Keymed, Inc.
Essex Ss2 5qh England, GB
Received
March 9, 1992
Decision date
March 29, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FEB – Accessories, Cleaning, For Endoscope
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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More from Medivators, Inc.

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K100803Olympus Flushing Pump Ofp Model: OFP-1FEQ · Special 04/22/2010SE
K881004Olympus-Keymed Endoscopic CO2 Regulator, Model EcrFCX · Traditional 05/12/1988SE
K861821Keymed Fiberscope Auto DisinfectorNVE · Traditional 02/12/1987SE
K864801The Keymed Hi-Light 250 Light SourceGCT · Traditional 12/24/1986SE
K862000Keymed Flexible Esophageal DilatorsKNQ · Traditional 08/12/1986SE
K860528The Keymed Fiberscope Sterilization CaseKCT · Traditional 07/15/1986SE
K861147UCS-2, Ultrasonic Cleaning SolutionFLG · Traditional 06/23/1986SE
K860704The Keymed Sigmoidoscope Disinfection StandNZA · Traditional 06/17/1986SE
K851149Key Med Transendoscopic Vascular Detector TVD-1JAF · Traditional 11/26/1985SE
K854304Keymed Office CouchFPO · Traditional 11/12/1985SE

Questions and answers

When was Olympus-Keymed Disinfectant Fume Extractor DFE-20 cleared by the FDA?

Olympus-Keymed Disinfectant Fume Extractor DFE-20 (K921179) received a 510(k) decision of Substantially Equivalent on March 29, 1993, 385 days after the submission was received.

What is the product code of K921179?

The FDA product code is FEB – Accessories, Cleaning, For Endoscope, a Class II (moderate risk) device regulated under 21 CFR 876.1500.