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FDA 510(k)

TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES

K-Number: K111736 · 2011-12-08

Decision Date2011-12-08
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES is the device name listed in this FDA 510(k) record. The listed applicant is Tuttnauer Co. , Ltd.. It received FDA 510(k) clearance on 2011-12-08 under 510(k) number K111736. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES?

TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES is a medical device that received FDA 510(k) clearance on 2011-12-08. The listed applicant is Tuttnauer Co. , Ltd.. The 510(k) number is K111736.

When did TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES receive FDA 510(k) clearance?

TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES received FDA 510(k) clearance on 2011-12-08, under 510(k) number K111736.

Who is the listed applicant for TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES?

The FDA 510(k) record lists Tuttnauer Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES?

The FDA product code for TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES 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 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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