Tuttnauer U.S.A Co, Ltd.
Tuttnauer U.S.A Co, Ltd. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2023.
Top product codes for Tuttnauer U.S.A Co, Ltd.
Recent clearances by Tuttnauer U.S.A Co, Ltd.
- K232658 — T-Top 10 & T-Top T-Top 11
- K143311 — Pre-vacuum Tabletop Autoclave
- K090783 — TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVE
- K032192 — PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS 4472 EP-1V AND 5596 EP-1V
- K021504 — TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540
- K993856 — TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EP
- K990761 — TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE
- K962282 — TUTTNAUER PREVACUUM TABLE AUTOCLAVE
- K973550 — TUTTNAUER TABLE-TOP AUTOCLAVE
Data sourced from openFDA. This site is unofficial and independent of the FDA.