BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9
K-Number: K060337 · 2006-03-08
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Device Summary
Frequently Asked Questions
What is the BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9?
BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9 is a medical device that received FDA 510(k) clearance on 2006-03-08. The listed applicant is Sauter AG. The 510(k) number is K060337.
When did BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9 receive FDA 510(k) clearance?
BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9 received FDA 510(k) clearance on 2006-03-08, under 510(k) number K060337.
Who is the listed applicant for BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9?
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 TOP 5000, MODEL 5-5-9?
The FDA product code for BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9 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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