Corplex P / Theracor P / Allacor P
K-Number: K231325 · 2024-02-02
Device Summary
Corplex P / Theracor P / Allacor P is a medical device manufactured by Stimlabs, LLC. It received FDA 510(k) clearance on 2024-02-02 under approval number K231325. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Corplex P / Theracor P / Allacor P?
Corplex P / Theracor P / Allacor P is a medical device that received FDA 510(k) clearance on 2024-02-02. It is manufactured by Stimlabs, LLC. The 510(k) number is K231325.
When was Corplex P / Theracor P / Allacor P approved by the FDA?
Corplex P / Theracor P / Allacor P received FDA 510(k) clearance on 2024-02-02, under approval number K231325.
What company makes Corplex P / Theracor P / Allacor P?
Corplex P / Theracor P / Allacor P is manufactured by Stimlabs, LLC.
What is the FDA product code for Corplex P / Theracor P / Allacor P?
The FDA product code for Corplex P / Theracor P / Allacor P is KGN.
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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.