BRAUN Silk.expert Pro 5
K-Number: K190354 · 2019-03-18
ApplicantCyden Limited
Decision Date2019-03-18
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
BRAUN Silk.expert Pro 5 is a medical device manufactured by Cyden Limited. It received FDA 510(k) clearance on 2019-03-18 under approval number K190354. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BRAUN Silk.expert Pro 5?
BRAUN Silk.expert Pro 5 is a medical device that received FDA 510(k) clearance on 2019-03-18. It is manufactured by Cyden Limited. The 510(k) number is K190354.
When was BRAUN Silk.expert Pro 5 approved by the FDA?
BRAUN Silk.expert Pro 5 received FDA 510(k) clearance on 2019-03-18, under approval number K190354.
What company makes BRAUN Silk.expert Pro 5?
BRAUN Silk.expert Pro 5 is manufactured by Cyden Limited.
What is the FDA product code for BRAUN Silk.expert Pro 5?
The FDA product code for BRAUN Silk.expert Pro 5 is OHT.
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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.