FDA 510(k)

아틀란 (A100); 아틀란 (A100 XL); 아틀란(A350); 아틀란 (A350 XL)

K-번호: K252746 · 2026-05-21

결정일2026-05-21

제품 코드BSZ

자문 위원회안내: 의료기기 규제 문서 번역 요청입니다. 회사명, 제품명, FDA, 510(k), PMA, NCT, PMID, 식별자 및 URL을 보존하여 번역하여 주세요. 정책: 의료규제-v1. [원문] AN [번역] 안내

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기기 요약

Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) is the device name listed in this FDA 510(k) record. The listed applicant is Drägerwerk AG Co. Kgaa. It received FDA 510(k) clearance on 2026-05-21 under 510(k) number K252746. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)?

Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) is a medical device that received FDA 510(k) clearance on 2026-05-21. The listed applicant is Drägerwerk AG Co. Kgaa. The 510(k) number is K252746.

When did Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) receive FDA 510(k) clearance?

Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) received FDA 510(k) clearance on 2026-05-21, under 510(k) number K252746.

Who is the listed applicant for Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)?

The FDA 510(k) record lists Drägerwerk AG Co. Kgaa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)?

The FDA product code for Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) is BSZ.

Drägerwerk AG Co. Kgaa를 신청인으로 등재한 기타 기록

K230931알란

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