BriefCase
K-Number: K221330 · 2022-11-18
Device Summary
Frequently Asked Questions
What is the BriefCase?
BriefCase is a medical device that received FDA 510(k) clearance on 2022-11-18. The listed applicant is Aidoc Medical , Ltd.. The 510(k) number is K221330.
When did BriefCase receive FDA 510(k) clearance?
BriefCase received FDA 510(k) clearance on 2022-11-18, under 510(k) number K221330.
Who is the listed applicant for BriefCase?
The FDA 510(k) record lists Aidoc Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BriefCase?
The FDA product code for BriefCase is QAS.
Other records listing Aidoc Medical , Ltd. 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: QAS)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.