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FDA 510(k)

BELIMED STEAM STERILIZER MST-V

K-Number: K130172 · 2013-09-23

ApplicantBelimed, Inc.
Decision Date2013-09-23
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 Belimed, Inc.. It received FDA 510(k) clearance on 2013-09-23 under 510(k) number K130172. 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 2013-09-23. The listed applicant is Belimed, Inc.. The 510(k) number is K130172.

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

BELIMED STEAM STERILIZER MST-V received FDA 510(k) clearance on 2013-09-23, under 510(k) number K130172.

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

The FDA 510(k) record lists Belimed, Inc. 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.

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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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