Medical Device Manufacturer · US , Washington , DC

Tuttnauer U.S.A Co, Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1997

Total

Cleared

Denied

Tuttnauer U.S.A Co, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2023. Active since 1997. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tuttnauer U.S.A Co, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Tuttnauer U.S.A Co, Ltd.

9 devices

1-9 of 9

Cleared Nov 27, 2023

T-Top 10 & T-Top T-Top 11

K232658 · FLE

General Hospital · 88d

Cleared Jan 15, 2015

Pre-vacuum Tabletop Autoclave

K143311 · FLE

General Hospital · 58d

Cleared Aug 20, 2009

TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVE

K090783 · FLE

General Hospital · 150d

Cleared Aug 12, 2004

PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS...

K032192 · FLE

General Hospital · 392d

Cleared Jul 25, 2002

TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540

K021504 · FLE

General Hospital · 77d

Cleared Feb 09, 2001

TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EP

K993856 · FLE

General Hospital · 452d

Cleared Jul 09, 1999

TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE

K990761 · FRG

General Hospital · 123d

Cleared Nov 12, 1997

TUTTNAUER PREVACUUM TABLE AUTOCLAVE

K962282 · FLE

General Hospital · 518d

Cleared Oct 29, 1997

TUTTNAUER TABLE-TOP AUTOCLAVE

K973550 · FLE

General Hospital · 41d

Tuttnauer U.S.A Co, Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Tuttnauer U.S.A Co, Ltd.

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