TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540
K-Number: K021504 · 2002-07-25
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Device Summary
Frequently Asked Questions
What is the TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540?
TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540 is a medical device that received FDA 510(k) clearance on 2002-07-25. The listed applicant is Tuttnauer U.S.A Co, Ltd.. The 510(k) number is K021504.
When did TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540 receive FDA 510(k) clearance?
TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540 received FDA 510(k) clearance on 2002-07-25, under 510(k) number K021504.
Who is the listed applicant for TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540?
The FDA 510(k) record lists Tuttnauer U.S.A Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540?
The FDA product code for TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540 is FLE.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Tuttnauer U.S.A Co, Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FLE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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