ABC D-FLEX PROBE
K-Number: K151229 · 2016-06-02
ApplicantConmed Corporation
Decision Date2016-06-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
ABC D-FLEX PROBE is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2016-06-02 under approval number K151229. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ABC D-FLEX PROBE?
ABC D-FLEX PROBE is a medical device that received FDA 510(k) clearance on 2016-06-02. It is manufactured by Conmed Corporation. The 510(k) number is K151229.
When was ABC D-FLEX PROBE approved by the FDA?
ABC D-FLEX PROBE received FDA 510(k) clearance on 2016-06-02, under approval number K151229.
What company makes ABC D-FLEX PROBE?
ABC D-FLEX PROBE is manufactured by Conmed Corporation.
What is the FDA product code for ABC D-FLEX PROBE?
The FDA product code for ABC D-FLEX PROBE is GEI.
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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.