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FDA 510(k)

EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870

K-Number: K003470 · 2001-02-20

Decision Date2001-02-20
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870 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 2001-02-20 under 510(k) number K003470. 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 EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870?

EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870 is a medical device that received FDA 510(k) clearance on 2001-02-20. The listed applicant is Tuttnauer Co. , Ltd.. The 510(k) number is K003470.

When did EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870 receive FDA 510(k) clearance?

EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870 received FDA 510(k) clearance on 2001-02-20, under 510(k) number K003470.

Who is the listed applicant for EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870?

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 EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870?

The FDA product code for EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870 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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