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FDA 510(k)

BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6

K-Number: K100622 · 2010-08-27

Decision Date2010-08-27
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6 is the device name listed in this FDA 510(k) record. The listed applicant is Belimed Sauter AG. It received FDA 510(k) clearance on 2010-08-27 under 510(k) number K100622. 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 BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6?

BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6 is a medical device that received FDA 510(k) clearance on 2010-08-27. The listed applicant is Belimed Sauter AG. The 510(k) number is K100622.

When did BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6 receive FDA 510(k) clearance?

BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6 received FDA 510(k) clearance on 2010-08-27, under 510(k) number K100622.

Who is the listed applicant for BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6?

The FDA 510(k) record lists Belimed Sauter AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6?

The FDA product code for BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6 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 Belimed Sauter AG 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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