Tuttnauer Electronic Autoclave, Models E, Ea, Ek, Eka, Ep

FDA 510(k) K993856 · Tuttnauer U.S.A Co, Ltd.

Substantially Equivalent

510(k) numberK993856

Submission

Device name
Tuttnauer Electronic Autoclave, Models E, Ea, Ek, Eka, Ep
Applicant
Tuttnauer U.S.A Co, Ltd.
Washington, DC, US
Received
November 15, 1999
Decision date
February 9, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FLE – Sterilizer, Steam
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6880
Specialty
General Hospital

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K243801FRONT-LINE Field Sterilizer (FL135)FLE · Special Fort Defiance Industries, LLC03/07/2025SE
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More from Primus Sterilizer Company, LLC

510(k)DeviceDecision
K232658T-Top 10 & T-Top T-Top 11FLE · Traditional 11/27/2023SE
K143311Pre-vacuum Tabletop AutoclaveFLE · Traditional 01/15/2015SE
K090783Tuttnauer ELARA-11 Pre-Vacuum Tabletop AutoclaveFLE · Traditional 08/20/2009SE
K032192Pre-Vacuum Autoclave with Steam Generator and Vertical Sliding Door, Models 4472 EP-1V…FLE · Abbreviated 08/12/2004SE
K021504Tuttnauer Ehs Series Table-Top Autoclave, Model 2540FLE · Abbreviated 07/25/2002SE
K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteFRG · Traditional 07/09/1999SE
K962282Tuttnauer Prevacuum Table AutoclaveFLE · Traditional 11/12/1997SE
K973550Tuttnauer Table-Top AutoclaveFLE · Traditional 10/29/1997SE

Questions and answers

When was Tuttnauer Electronic Autoclave, Models E, Ea, Ek, Eka, Ep cleared by the FDA?

Tuttnauer Electronic Autoclave, Models E, Ea, Ek, Eka, Ep (K993856) received a 510(k) decision of Substantially Equivalent on February 9, 2001, 452 days after the submission was received.

What is the product code of K993856?

The FDA product code is FLE – Sterilizer, Steam, a Class II (moderate risk) device regulated under 21 CFR 880.6880.