FDA 510(k)

Konig Bell Circumcision Clamp

Número K: K251687 · 2026-02-25

Data da decisão2026-02-25

Código do produtoHFX

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

Konig Bell Circumcision Clamp is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, LP. It received FDA 510(k) clearance on 2026-02-25 under 510(k) number K251687. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Konig Bell Circumcision Clamp?

Konig Bell Circumcision Clamp is a medical device that received FDA 510(k) clearance on 2026-02-25. The listed applicant is Medline Industries, LP. The 510(k) number is K251687.

When did Konig Bell Circumcision Clamp receive FDA 510(k) clearance?

Konig Bell Circumcision Clamp received FDA 510(k) clearance on 2026-02-25, under 510(k) number K251687.

Who is the listed applicant for Konig Bell Circumcision Clamp?

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

What is the FDA product code for Konig Bell Circumcision Clamp?

The FDA product code for Konig Bell Circumcision Clamp is HFX.

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Fonte oficial

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