RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed
K-Number: K161737 · 2017-03-02
ApplicantMyco Medical
Decision Date2017-03-02
Product CodeNEW
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is a medical device manufactured by Myco Medical. It received FDA 510(k) clearance on 2017-03-02 under approval number K161737. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is a medical device that received FDA 510(k) clearance on 2017-03-02. It is manufactured by Myco Medical. The 510(k) number is K161737.
When was RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed approved by the FDA?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed received FDA 510(k) clearance on 2017-03-02, under approval number K161737.
What company makes RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is manufactured by Myco Medical.
What is the FDA product code for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
The FDA product code for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is NEW.
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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.