Compass Cast and MAP
K-Number: K161408 · 2016-11-22
Decision Date2016-11-22
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Compass Cast and MAP is a medical device manufactured by Centurion Medical Products Corporation. It received FDA 510(k) clearance on 2016-11-22 under approval number K161408. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Compass Cast and MAP?
Compass Cast and MAP is a medical device that received FDA 510(k) clearance on 2016-11-22. It is manufactured by Centurion Medical Products Corporation. The 510(k) number is K161408.
When was Compass Cast and MAP approved by the FDA?
Compass Cast and MAP received FDA 510(k) clearance on 2016-11-22, under approval number K161408.
What company makes Compass Cast and MAP?
Compass Cast and MAP is manufactured by Centurion Medical Products Corporation.
What is the FDA product code for Compass Cast and MAP?
The FDA product code for Compass Cast and MAP is DRS.
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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.