FDA 510(k)

콜라겐 P.I.N. (피부 내 유도 주사)

K-번호: K222199 · 2022-10-21

결정일2022-10-21

제품 코드QAI

자문 위원회SU [원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

결정대체적으로 동일

기기 요약

Collagen P.I.N. (Percutaneous Induction Needling) is the device name listed in this FDA 510(k) record. The listed applicant is Induction Therapies, LLC. It received FDA 510(k) clearance on 2022-10-21 under 510(k) number K222199. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Collagen P.I.N. (Percutaneous Induction Needling)?

Collagen P.I.N. (Percutaneous Induction Needling) is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Induction Therapies, LLC. The 510(k) number is K222199.

When did Collagen P.I.N. (Percutaneous Induction Needling) receive FDA 510(k) clearance?

Collagen P.I.N. (Percutaneous Induction Needling) received FDA 510(k) clearance on 2022-10-21, under 510(k) number K222199.

Who is the listed applicant for Collagen P.I.N. (Percutaneous Induction Needling)?

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

What is the FDA product code for Collagen P.I.N. (Percutaneous Induction Needling)?

The FDA product code for Collagen P.I.N. (Percutaneous Induction Needling) is QAI.

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콜라겐 P.I.N. (피부 내 유도 주사)

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: QAI)

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