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FDA 510(k)

BELIMED STEAM STERILIZER MST-V

K-Number: K103841 · 2011-03-15

ApplicantSauter AG
Decision Date2011-03-15
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BELIMED STEAM STERILIZER MST-V is the device name listed in this FDA 510(k) record. The listed applicant is Sauter AG. It received FDA 510(k) clearance on 2011-03-15 under 510(k) number K103841. 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 MST-V?

BELIMED STEAM STERILIZER MST-V is a medical device that received FDA 510(k) clearance on 2011-03-15. The listed applicant is Sauter AG. The 510(k) number is K103841.

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

BELIMED STEAM STERILIZER MST-V received FDA 510(k) clearance on 2011-03-15, under 510(k) number K103841.

Who is the listed applicant for BELIMED STEAM STERILIZER MST-V?

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

What is the FDA product code for BELIMED STEAM STERILIZER MST-V?

The FDA product code for BELIMED STEAM STERILIZER MST-V 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 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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