FDA 510(k)

VERIQA

K 號：K213370 · 2022-03-30

申請人Ptw-Freiburg Physikalisch-Technische-Werkstaetten

決定日期2022-03-30

產品代碼IYE

諮詢委員會RA

決定相當於

器材摘要

VERIQA is the device name listed in this FDA 510(k) record. The listed applicant is Ptw-Freiburg Physikalisch-Technische-Werkstaetten. It received FDA 510(k) clearance on 2022-03-30 under 510(k) number K213370. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the VERIQA?

VERIQA is a medical device that received FDA 510(k) clearance on 2022-03-30. The listed applicant is Ptw-Freiburg Physikalisch-Technische-Werkstaetten. The 510(k) number is K213370.

When did VERIQA receive FDA 510(k) clearance?

VERIQA received FDA 510(k) clearance on 2022-03-30, under 510(k) number K213370.

Who is the listed applicant for VERIQA?

The FDA 510(k) record lists Ptw-Freiburg Physikalisch-Technische-Werkstaetten as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERIQA?

The FDA product code for VERIQA is IYE.

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官方來源

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