FDA 510(k)

Corplex P / Theracor P / Allacor P

K-Number: K231325 · 2024-02-02

Decision Date2024-02-02

Product CodeKGN

DecisionSubstantially Equivalent

Device Summary

Corplex P / Theracor P / Allacor P is the device name listed in this FDA 510(k) record. The listed applicant is Stimlabs, LLC. It received FDA 510(k) clearance on 2024-02-02 under 510(k) 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. The listed applicant is Stimlabs, LLC. The 510(k) number is K231325.

When did Corplex P / Theracor P / Allacor P receive FDA 510(k) clearance?

Corplex P / Theracor P / Allacor P received FDA 510(k) clearance on 2024-02-02, under 510(k) number K231325.

Who is the listed applicant for Corplex P / Theracor P / Allacor P?

The FDA 510(k) record lists Stimlabs, LLC as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Stimlabs, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253339Theracor K242828Corplex P/ Theracor P/ Allacor P

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.