BELIMED STEAM STERILIZER MST-V
K-Number: K103841 · 2011-03-15
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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