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FDA 510(k)

VERIQA

K-Number: K213370 · 2022-03-30

Decision Date2022-03-30
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Ptw-Freiburg Physikalisch-Technische-Werkstaetten 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.

Related Devices (Code: IYE)

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.

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.